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Red Delicious Apple

Nelco Laboratories, Inc.
Nelco Laboratories, Inc.

Allergenic Extract


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

WARNING

Diagnostic and therapeutic allergenic extracts are intended to be administered by a physician who is an allergy specialist and experienced in allergenic diagnostic testing and immunotherapy and the emergency care of anaphylaxis.

This product should not be injected intravenously. Deep subcutaneous routes have been safe. Sensitive patients may experience severe anaphylactic reactions resulting in respiratory obstruction, shock, coma and/or death. (See Adverse Reactions)

Serious adverse reactions should be reported to Nelco Laboratories immediately and a report filed to: MedWatch, The FDA Medical Product Problem Reporting Program, at 5600 Fishers Lane, Rockville, Md. 20852-9787, call 1-800-FDA-1088.

Extreme caution should be taken when using allergenic extracts for patients who are taking beta-blocker medications. In the event of a serious adverse reaction associated with the use of allergenic extracts, patients receiving beta-blockers may not be responsive to epinephrine or inhaled brochodialators.(1) (See Precautions)

Allergenic extracts should be used with caution for patients with unstable or steroid-dependent asthma or underlying cardiovascular disease. (See Contraindications)

RED DELICIOUS APPLE DESCRIPTION

Allergenic extracts are sterile solutions consisting of the extractable components from various biological sources including pollens, inhalants, molds, animal epidermals and insects. Aqueous extracts are prepared using cocas fluid containing NaCl 0.5%, NaHCO3 0.0275%, WFI, preservative 0.4% Phenol. Glycerinated allergenic extracts are prepared with cocas fluid and glycerin to produce a 50% (v/v) allergenic extract. Allergenic Extracts are supplied as concentrations designated as protein nitrogen units (PNU) or weight/volume (w/v) ratio. Standardized extracts are designated in Bioequivalent Allergy Units (BAU) or Allergy Units (AU). (See product insert for standardized extracts)

For diagnostic purposes, allergenic extracts are to be administered by prick-puncture or intradermal routes. Allergenic extracts are administered subcutaneously for immunotherapy injections.

CLINICAL PHARMACOLOGY

The pharmacological action of allergenic extracts used diagnostically is based on the liberation of histamine and other substances when the allergen reacts with IgE antibodies attached to the mast cells. When allergenic extracts are used for immunotherapy, the effect is an increase in immunoglobulin G (IgG) and an increased T suppresser lymphocyte which interferes with the allergic response.(2) With repeated administration of allergenic extracts changes develop in regards to IgG and IgE production and mediator-releasing cells. The histamine release response is reduced in some patients.

RED DELICIOUS APPLE INDICATIONS AND USAGE

Allergenic extracts are indicated for use in diagnostic testing and as part of a treatment regime for allergic disease, as established by allergy history and skin test reactivity.

Allergenic extracts are indicated for the treatment of allergen specific allergic disease for use as hyposensitization or immunotherapy when avoidance of specific allergens can not be attained. The use of allergenic extracts for therapeutic purpose has been established by well-controlled clinical studies. Allergenic extracts may be used as adjunctive therapy along with pharmacotherapy which includes antihistamines, corticosteroids, and cromoglycate, and avoidance measures. Allergenic extracts for therapeutic use should be given using only the allergen selection to which the patient is allergic, has a history of exposure and are likely to be exposed to again.

RED DELICIOUS APPLE CONTRAINDICATIONS

Allergenic extracts should not be used if the patient has asthma, cardiovascular disease, emphysema, diabetes, bleeding diathesis or pregnancy, unless a specific diagnosis of type 1 allergic disease is made based on skin testing and the benefits of treatment outweigh the risks of an adverse reaction during testing or treatment. Allergenic extracts are not indicated for use in patients who are not clinically allergic or who are not skin reactive to an allergen. Allergenic extracts should be discontinued or the concentration of potency substantially reduced in patients who experience unacceptable adverse reactions.

WARNINGS

DO NOT INJECT INTRAVENOUSLY.

Epinephrine 1:1000 should be available.

Concentrated extracts must be diluted with sterile diluent prior to first use on a patient for treatment or intradermal testing. All concentrates of glycerinated allergenic extracts have the ability to cause serious local and systemic reactions including death in sensitive patients. Sensitive patients may experience severe anaphylactic reactions resulting in respiratory obstruction, shock, coma and /or death.(4) (See Adverse Reactions) An allergenic extract should be temporarily withheld from patients or the dose of the extract adjusted downward if any of the following conditions exist: (1) Severe symptoms of rhinitis and/or asthma (2) Infections or flu accompanied by fever and (3) Exposure to excessive amounts of clinically relevant allergen prior to a scheduled injection. When switching patients to a new lot of the same extract the initial dose should be reduced 3/4 so that 25% of previous dose is administered.

PRECAUTIONS

GENERAL: Epinephrine 1:1000 should be available as well as personnel trained in administering emergency treatment. Allergenic Extracts are not intended for intravenous injections. For safe and effective use of allergenic extracts, sterile diluents, sterile vials, sterile syringes should be used and aseptic precautions observed when making a dilution and/or administering the allergenic extract injection. A sterile tuberculin syringe graduated in 0.1 ml units to measure each dose for the prescribed dilution should be used. To reduce the risk of an occurrence of adverse reactions, begin with a careful personal history plus a physical exam. Confirm your findings with scratch or intradermal skin testing.

Standardized extracts are those labeled in AU/ml units or BAU/ml units. Standardized extracts are not interchangeable with extracts previously labeled as wt/vol or PNU/ml. Before administering a standardized extract, read the accompanying insert contained with standardized extracts.

Information for Patients: All concentrates of allergenic extracts have the ability to cause serious local and systemic reactions including death in sensitive patients. Patients should be informed of this risk prior to skin testing and immunotherapy. Patients should be instructed to recognize adverse reaction symptoms that may occur and to report all adverse reactions to a physician. Patients should be instructed to remain in the office for 30 minutes during testing using allergenic extracts and at least 30 minutes after therapeutic injections using allergenic extracts.

DRUG INTERACTIONS: Some drugs may affect the reactivity of the skin; patients should be instructed to avoid medications, particularly antihistamines and sympathomimetic drugs, for at least 24 hours prior to skin testing. Antihistamines and Hydroxyzine can significantly inhibit the immediate skin test reactions as they tend to neutralize or antagonize the action of histamine.(3) This effect has been primarily documented when testing was performed within 1 to 2 hours after drug ingestion. Partial inhibition of the skin test reaction had been observed for longer periods. Epinephrine injection inhibits the immediate skin test reactions for several hours. Patients on delayed absorption antihistamine tablets should be free of such medication for 48 hours before testing. Patients using Astemizole (Hismanal) may experience prolonged suppression and should be free from such medication for up to 6 to 8 weeks prior to testing. Refer to package insert from an applicable long acting antihistamine manufacturer for additional information.

Extreme caution should be taken when using allergenic extracts on patients who are taking beta-blockers. Patients on non-selective beta blockers may be more reactive to allergens given for testing or treatment and may be unresponsive to the usual doses of epinephrine used to treat allergic reactions.

Carcinogenesis, mutagenesis, impairment of fertility:

Long term studies in animals have not been conducted with allergenic extracts to determine their potential carcinogenicity, mutagenicity or impairment of fertility.

Pregnancy: Category C: Animal reproduction studies have not been conducted with Allergenic Extracts. It is not known whether allergenic extracts can cause fetal harm when administered to pregnant women or can affect reproduction capacity. Allergenic extracts should be given to pregnant women only if clearly needed.

Nursing Mothers: It is not known whether this drug appears in human milk. Because many drugs are detected in human milk, caution should be exercised when Allergenic Extracts are administered to a nursing woman. There are no current studies on extract components in human milk, or their effect on the nursing infant.

Pediatric Use: Allergenic extracts have been used in children over two years of age.(5)

RED DELICIOUS APPLE ADVERSE REACTIONS

Adverse systemic reactions usually occur within minutes and consist primarily of allergic symptoms such as: generalized skin erythema, urticaria, pruritus, angioedema, rhinitis, wheezing, laryngeal edema, itching of nose and throat, breathlessness, dyspnea, coughing, hypotension and marked perspiration. Less commonly, nausea, emesis, abdominal cramps, diarrhea and uterine contractions may occur. Severe reactions may cause anaphylaxis or shock and loss of consciousness and rarely death.

The treatment of systemic allergic reactions is dependent upon the system complex. Antihistamines may offer relief of recurrent urticaria, associated skin reactions and gastrointestinal symptoms. Corticosteroids may provide benefit if symptoms are prolonged or recurrent. (See Overdose section)

Local Reactions consisting of erythema, itching, swelling tenderness and sometimes pain may occur at the injection site. These reactions may appear within a few minutes to hours and persist for several days. Local cold applications and oral antihistamines may be effective treatment. For marked and prolonged local reactions the use of antihistamines or anti-inflammatory medications may be dictated. Serious adverse reactions should be reported to Nelco Laboratories immediately and a report can be filed to: MedWatch, The FDA Medical Product Problem Reporting Program, at 5600 Fishers Lane, Rockville, MD 20852-9787, call 1-800-FDA-1088.

OVERDOSAGE

Overdose can cause both local and systemic reactions. An overdose may be prevented by careful observation and questioning of the patient about the previous injection.

If systemic or anaphylactic reaction, does occur, apply a tourniquet above the site of injection and inject intramuscularly or subcutaneously 0.3 to 0.5ml of 1:1000 Epinephrine Hydrochloride into the opposite arm. The dose may be repeated in 5-10 minutes if necessary. Loosen the tourniquet at least every 10 minutes. The Epinephrine Hydrochloride 1:1000 dose for infants to 2 years is 0.05 to 0.1 ml, for children 2 to 6 years it is 0.15 ml, for children 6-12 years it is 0.2 ml.

Patients unresponsive to Epinephrine may be treated with Theophylline. Studies on asthmatic subjects reveal that plasma concentrations of Theophylline of 5 to 20 µg/ml are associated with therapeutic effects. Toxicity is particularly apparent at concentrations greater than 20 µg/ml. A loading dose of Aminophylline of 5.8 mg/kg intravenously followed by 0.9 mg/kg per hour results in plasma concentrations of approximately 10 µg/ml for patients not previously receiving theophylline. (Mitenko and Ogilive, Nicholoson and Chick,1973)

Other beta-adrenergic drugs such as Isoproterenol, Isoetharine, or Albuterol may be used by inhalation. The usual dose to relieve broncho-constriction in asthma is 0.5 ml of the 0.5% solution for Isoproterenol HCl. The Albuterol inhaler delivers approximately 90 mcg of Albuterol from the mouthpiece. The usual dosage for adults and children would be two inhalations repeated every 4-6 hours. Isoetharine supplied in the Bronkometer unit delivers approximately 340 mcg Isoetharine. The average dose is one to two inhalations. Respiratory obstruction not responding to parenteral or inhaled bronchodilators may require oxygen, intubation and the use of life support systems.

RED DELICIOUS APPLE DOSAGE AND ADMINISTRATION

General Precautions

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permits.

The dosage of allergenic extracts is dependent upon the purpose of the administration. Allergenic extracts can be administered for diagnostic use or for therapeutic use.

When allergenic extracts are administered for diagnostic use, the dosage is dependent upon the method used. Two methods commonly used are scratch testing and intradermal testing. Both types of tests result in a wheal and flare response at the site of the test which usually develops rapidly and may be read in 20-30 minutes.

Diagnostic Use : Scratch Testing Method

Scratch testing is considered a simple and safe method although less sensitive than the intradermal test. Scratch testing can be used to determine the degree of sensitivity to a suspected allergen before using the intradermal test. This combination lessens the severity of response to an allergen which can occur in a very sensitive patient.

The most satisfactory testing site is the patient's back or volar surface of the arms from the axilla to 2.5 or 5cm above the wrist, skipping the anti-cubital space. If using the back as a testing site, the most satisfactory area are from the posterior axillary fold to 2.5 cm from the spinal column, and from the top of the scapula to the lower rib margins.

Allergenic extracts for diagnostic use are to be administered in the following manner: To scratch surface of skin, use a circular scarifier. Do not draw blood. Tests sites should be 4 cm apart to allow for wheal and flare reaction. 1-30 scratch tests may be done at a time. A separate sterile scratch instrument is to be used on each patient to prevent transmission of homologous serum hepatitis or other infectious agents from one patient to another.

The recommended usual dosage for Scratch testing is one drop of allergen applied to each scratch site. Do not let dropper touch skin. Always apply a control scratch with each test set. Sterile Diluent (for a negative control) is used in exactly the same way as an active test extract. Histamine may be used as a positive control. Scratch or prick test sites should be examined at 15 and 30 minutes. To prevent excessive absorption, wipe off antigens producing large reactions as soon as the wheal appears. Record the size of the reaction.

Interpretation of Scratch Test

Skin tests are graded in terms of the wheal and erythema response noted at 10 to 20 minutes. Wheal and erythema size may be recorded by actual measurement as compared with positive and negative controls. A positive reaction consists of an area of erythema surrounding the scarification that is larger than the control site. For uniformity in reporting reactions, the following system is recommended. (6)

REACTION SYMBOL CRITERIA
Negative - No wheal. Erythema absent or very slight (not more than 1 mm diameter).
One Plus + Wheal absent or very slight erythema present (not more than 3 mm diameter).
Two Plus ++ Wheal not more than 3mm or erythema not more than 5mm diameter.
Three Plus +++ Wheal between 3mm and 5mm diameter, with erythema. Possible pseudopodia and itching.
Four Plus ++++ A larger reaction with itching and pain.

Diagnostic Use: Intradermal Skin Testing Method

Do not perform intradermal test with allergens which have evoked a 2+ or greater response to a Scratch test. Clean test area with alcohol, place sites 5 cm apart using separate sterile tuberculin syringe and a 25 gauge needle for each allergen. Insert needle tip, bevel up, into intracutaneous space. Avoid injecting into blood vessel, pull back gently on syringe plunger, if blood enters syringe change position of needle. The recommended dosage and range for intradermal testing is 0.05 ml of not more than 100 pnu/ml or 1:1000 w/v (only if puncture test is negative) of allergenic extract. Inject slowly until a small bleb is raised. It is important to make each bleb the same size.

Interpretation of Intradermal Test:

The patient's reaction is graded on the basis of size of wheal and flare as compared to control. Use 0.05 ml sterile diluent as a negative control to give accurate interpretation. The tests may be accurately interpreted only when the saline control site has shown a negative response. Observe patient for at least 30 minutes. Tests can be read in 15-20 minutes. Edema, erythema and presence of pseudopods, pain and itching may be observed in 4 plus reactions. For uniformity in reporting reactions the following system is recommended. (6)

REACTION SYMBOL CRITERIA
Negative - No increase in size of bleb since injection. No erythema.
One Plus + An increase in size of bleb to a wheal not more than 5mm diameter, with associated erythema.
Two Plus ++ Wheal between 5mm and 8mm diameter with erythema.
Three Plus +++ Wheal between 8mm and 12mm diameter with erythema and possible pseudopodia and itching or pain.
Four Plus ++++ Any larger reaction with itch and pain, and possible diffuse blush of the skin surrounding the reaction area.

Therapeutic Use: Recommended dosage & range

Check the listed ingredients to verify that it matches the prescription ordered. When using a prescription set, verify the patient's name and the ingredients listed with the prescription order. Assess the patient's physical and emotional status prior to giving as injection. Do not give injections to patients who are in acute distress. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

Dosage of allergenic extracts is a highly individualized matter and varies according to the degree of sensitivity of the patient, his clinical response and tolerance to the extract administered during the early phases of an injection regimen. The dosage must be reduced when transferring a patient from non-standardized or modified extract to standardized extract. Any evidence of a local or generalized reaction requires a reduction in dosage during the initial stages of immunotherapy as well as during maintenance therapy. After therapeutic injections patients should be observed for at least 20 minutes for reaction symptoms.

SUGGESTED DOSAGE SCHEDULE

The following schedule may act as a guide. This schedule has not been proven to be safe or effective. Sensitive patients may begin with smaller doses of weaker solutions and the dosage increments can be less.

STRENGTH DOSE VOLUME
Vial #1 1 0.05
1:100,000 w/v 2 0.10
10 pnu/ml 3 0.15
1 AU/ml 4 0.20
1 BAU/ml 5 0.30
6 0.40
7 0.50
Vial #2 8 0.05
1:10,000 w/v 9 0.10
100 pnu/ml 10 0.15
10 AU/ml 11 0.20
10 BAU/ml 12 0.30
13 0.40
14 0.50
Vial #3 15 0.05
1:1,000 w/v 16 0.10
1,000 pnu/ml 17 0.15
100 AU/ml 18 0.20
100 BAU/ml 19 0.30
20 0.40
21 0.50
Vial #4 22 0.05
1:100 w/v 23 0.07
10,000 pnu/ml 24 0.10
1,000 AU/ml 25 0.15
1,000 BAU/ml 26 0.20
27 0.25
Maintenance Refill 28 0.25
1:100 w/v 29 0.25
10,000 pnu/ml 30 0.25
1,000 AU/ml 31 0.25
1,000 BAU/ml 32 0.25
subsequent doses 33 0.25

Preparation Instructions:

All dilutions may be made using sterile buffered diluent. The calculation may be based on the following ratio:

Volume desired x Concentration desired = Volume needed x Concentration available.

Example 1: If a 1:10 w/v extract is available and it is desired to use a 1:1,000 w/v extract substitute as follows:

Vd x Cd = Vn x Ca

10ml x 0.001 = Vn x 0.1

0.1 ml = Vn

Using a sterile technique, remove 0.10 ml of extract from the 1:10 vial and place it into a vial containing 9.90 ml of sterile diluent. The resulting ratio will be a 10 ml vial of 1:1,000 w/v.

Example 2: If a 10,000 pnu/ml extract is available and it is desired to use a 100 pnu/ml extract substitute as follows:

10ml x 100 = Vn x 10,000

0.1 ml = Vn

Using a sterile technique, remove 0.10 ml of extract from the 10,000 pnu/ml vial and place it into a vial containing 9.90 ml of sterile diluent. The resulting concentration will be a 10 ml vial of 100 pnu/ml.

Example 3: If a 10,000 AU/ml or BAU/ml extract is available and it is desired to use a 100 AU/ml or BAU/ml extract substitute as follows: Vd x Cd = Vn x Ca

10ml x 100 = Vn x 10,000

0.1 ml = Vn

Using a sterile technique, remove 0.10 ml of extract from the 10,000 AU/ml or BAU/ml vial and place it into a vial containing 9.90 ml of sterile diluent. The resulting concentration will be 10ml vial of 100 AU/ml or BAU/ml.

Intervals between doses: The optimal interval between doses of allergenic extract has not been definitely established. The amount of allergenic extract is increased at each injection by not more than 50%-100% of the previous amount and the next increment is governed by the response to the last injection. There are three generally accepted methods of pollen hyposensitizing therapy.

1. PRESEASONAL

Treatment starts each year 6 to 8 weeks before onset of seasonal symptoms. Maximal dose reached just before symptoms are expected. Injections discontinued during and following season until next year.

2. CO-SEASONAL

Patient is first treated during season with symptoms. Low initial doses are employed to prevent worsening of condition. This is followed by an intensive schedule of therapy (i.e. injections given 2 to 3 times per week). Fewer Allergists are resorting to this Co-seasonal therapy because of the availability of more effective, symptomatic medications that allow the patient to go through a season relatively symptom free.

3. PERENNIAL

Initially this is the same as pre seasonal. The allergen is administered twice weekly or weekly for about 20 injections to achieve the maximum tolerated dose. Then, maintenance therapy may be administered once a week or less frequently.

Duration of Treatment: The usual duration of treatment has not been established. A period of two or three years of injection therapy constitutes an average minimum course of treatment.

HOW SUPPLIED

Allergenic extracts are supplied with units listed as: Weight/volume (W/V), Protein Nitrogen Units (PNU/ml), Allergy Units (AU/ml) or Bioequivalent Allergy Units (BAU/ml).

Sizes:

Diagnostic Scratch: 5 ml dropper application vials

Diagnostic Intradermal: 5 ml or 10 ml vials.

Therapeutic Allergens: 5 ml, 10 ml, 50 ml multiple dose vials.

STORAGE

The expiration date of allergen extracts is listed on the container label. Store extracts upon arrival at 2° to 8°C and keep them in this range during office use.

WARRANTY: We warrant that this product was prepared and tested according to the standards of the FDA and is true to label. Because of biological differences in individuals and because allergenic extracts are manufactured to be potent and because we have no control over the conditions of use, we cannot and do not warrant either a good effect or against an ill effect following use.

REFERENCES

1 Jacobs, Robert L., Geoffrey W.Rake,Jr., et.al. Potentiated Anaphylaxis in Patients with Drug-induced Beta-adrenergic Blockade. J.Allergy & Clin. Immunol., 68(2): 125-127. August 1981.

2 Ishizaka,K.: Cellular Events in the IgE Antibody Response. Adv. in Immuno. 23:50-75, 1976.

3. Lockey, R.F., Bukantz, S.C., Allergen Immunotherapy. New York,NY: Marcel Dekker Inc., 1991.

4. Reid,M.J., Lockey,R.F., Turkeltaub,P.C., Platts-Mills,T.A.E., Survey of fatalities from skin testing and immunotherapy 1985-1989. Journal of Allergy Clin. Immunol. 92 (1): 6-15, July 1993.

5. Murray, A.B., Ferguson, A., Morrison, B., The frequency and severity of cat allergy vs dog allergy in atopic children. J. Allergy Clin. Immunolo: 72, 145-9, 1983.

6. Lockey, R.F., Bukantz, S.C., Allergen Immunotherapy. New York,NY: Marcel Dekker Inc., 1991.

CONTAINER LABELING

Red Delicious Apple

Red Delicious Apple INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1284
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
APPLE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1284-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1284-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1284-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1284-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Apricot

Apricot INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1288
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
APRICOT 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
water
PHENOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1288-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1288-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1288-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1288-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Avocado

Avocado INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1292
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOCADO 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1292-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1292-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1292-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1292-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Banana

Banana INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1296
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BANANA 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1296-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1296-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1296-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1296-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Blackberry

Blackberry INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1300
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BLACKBERRY 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1300-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1300-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1300-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1300-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Blueberry

Blueberry INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1304
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BLUEBERRY 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1304-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1304-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1304-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1304-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Cantaloupe

Cantaloupe INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1308
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CANTALOUPE Cantaloupe 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1308-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1308-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1308-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1308-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Cherry Bing

Cherry Bing INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1312
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SOUR CHERRY SOUR CHERRY 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1312-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1312-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1312-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1312-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Cranberry

Cranberry INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1316
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CRANBERRY CRANBERRY 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1316-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1316-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1316-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1316-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Date

Date INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1320
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DATE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1320-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1320-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1320-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1320-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Fig

Fig INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1324
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
FIG 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1324-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1324-2 0.1 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1324-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1324-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Grapefruit

Grapefruit INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1332
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
GRAPEFRUIT 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1332-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1332-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1332-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1332-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Honeydew Melon

Honeydew Melon INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1336
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HONEYDEW MELON HONEYDEW MELON 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1336-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1336-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1336-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1336-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Lemon

Lemon INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1340
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LEMON 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1340-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1340-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1340-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1340-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Lime

Lime INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1344
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LIME (CITRUS) 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1344-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1344-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1344-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1344-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Orange

Orange INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1348
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ORANGE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1348-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1348-2 30 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1348-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1348-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Peach

Peach INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1352
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PEACH Peach 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1352-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1352-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1352-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1352-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Pear

Pear INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1356
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PEAR 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1356-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1356-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1356-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1356-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Pineapple

Pineapple INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1360
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PINEAPPLE PINEAPPLE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1360-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1360-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1360-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1360-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Plum

Plum INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1364
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PLUM PLUM 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1364-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1364-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1364-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1364-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Raspberry

Raspberry INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1368
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
RASPBERRY 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1368-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1368-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1368-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1368-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Strawberry

Strawberry INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1372
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Strawberry 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1372-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1372-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1372-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1372-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Tangerine

Tangerine INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1376
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TANGERINE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1376-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1376-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1376-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1376-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Watermelon

Watermelon INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1380
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
WATERMELON 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1380-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1380-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1380-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1380-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Artichoke

Artichoke INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1384
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ARTICHOKE ARTICHOKE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1384-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1384-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1384-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1384-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Asparagus

Asparagus INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1388
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ASPARAGUS ASPARAGUS 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1388-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1388-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1388-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1388-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Red Kidney Beans

Red Kidney Beans INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1392
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
KIDNEY BEAN KIDNEY BEAN 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1392-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1392-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1392-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1392-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Lima Beans

Lima Beans INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1396
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LIMA BEAN 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1396-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1396-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1396-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1396-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Navy Beans

Navy Beans INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1400
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
KIDNEY BEAN KIDNEY BEAN 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1400-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1400-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1400-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1400-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


String Beans

String Beans INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1404
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
STRING BEAN String Bean 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1404-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1404-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1404-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1404-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Beet

Beet INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1408
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BEET 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1408-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1408-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1408-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1408-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Broccoli

Broccoli INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1412
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BROCCOLI BROCCOLI 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1412-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1412-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1412-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1412-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Kiwi

Kiwi INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1416
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
KIWI FRUIT 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1416-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1416-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1416-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1416-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Brussels Sprout

Brussels Sprout INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1420
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BRUSSELS SPROUT BRUSSELS SPROUT 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1420-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1420-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1420-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1420-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Cabbage

Cabbage INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1424
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CABBAGE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1424-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1424-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1424-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1424-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Carrot

Carrot INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1428
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CARROT 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1428-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1428-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1428-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1428-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Cauliflower

Cauliflower INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1432
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CAULIFLOWER CAULIFLOWER 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1432-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1432-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1432-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1432-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Celery

Celery INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1436
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CELERY Celery 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1436-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1436-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1436-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1436-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Sweet Corn

Sweet Corn INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1440
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CORN 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1440-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1440-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1440-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1440-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Cucumber

Cucumber INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1444
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CUCUMBER 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1444-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1444-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1444-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1444-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Egg Plant

Egg Plant INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1448
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
EGGPLANT 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1448-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1448-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1448-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1448-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Green Pepper

Green Pepper INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1452
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
GREEN BELL PEPPER Green Bell Pepper 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1452-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1452-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1452-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1452-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Lentil

Lentil INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1456
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LENTIL 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1456-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1456-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1456-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1456-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Iceberg Lettuce

Iceberg Lettuce INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1460
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LETTUCE LETTUCE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1460-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1460-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1460-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1460-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Mushroom

Mushroom INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1464
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CULTIVATED MUSHROOM 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1464-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1464-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1464-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1464-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Black Olive

Black Olive INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1468
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BLACK OLIVE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1468-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1468-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1468-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1468-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Green Olive

Green Olive INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1472
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
GREEN OLIVE GREEN OLIVE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1472-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1472-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1472-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1472-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Yellow Onion

Yellow Onion INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1476
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ONION ONION 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1476-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1476-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1476-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1476-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Parsley

Parsley INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1480
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PARSLEY 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1480-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1480-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1480-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1480-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Green Pea

Green Pea INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1484
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PEA 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1484-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1484-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1484-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1484-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Sweet Potato

Sweet Potato INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1488
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SWEET POTATO 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1488-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1488-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1488-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1488-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


White Potato

White Potato INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1492
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
POTATO Potato 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1492-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1492-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1492-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1492-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Pumpkin

Pumpkin INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1496
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALLERGENIC EXTRACT- PUMPKIN CUCURBITA PEPO ALLERGENIC EXTRACT- PUMPKIN CUCURBITA PEPO 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1496-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1496-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1496-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1496-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Radish

Radish INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1500
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
RAPHANUS SATIVUS DAIKON 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1500-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1500-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1500-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1500-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Rhubarb

Rhubarb INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1504
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
RHUBARB 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1504-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1504-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1504-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1504-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Soybean

Soybean INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1508
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SOYBEAN 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1508-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1508-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1508-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1508-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Spinach

Spinach INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1512
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SPINACH SPINACH 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1512-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1512-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1512-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1512-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Squash Zucchini

Squash Zucchini INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1516
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SQUASH SQUASH 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1516-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1516-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1516-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1516-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Tomato

Tomato INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1520
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TOMATO 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1520-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1520-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1520-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1520-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Turnip

Turnip INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1524
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TURNIP TURNIP 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1524-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1524-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1524-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1524-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Almond

Almond INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1528
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALMOND 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1528-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1528-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1528-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1528-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Brazil Nut

Brazil Nut INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1532
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BRAZIL NUT Brazil Nut 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1532-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1532-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1532-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1532-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Cashew

Cashew INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1536
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CASHEW Cashew 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1536-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1536-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1536-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1536-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Coconut

Coconut INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1540
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
COCONUT 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1540-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1540-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1540-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1540-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


English Walnut

English Walnut INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1544
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ENGLISH WALNUT English Walnut 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1544-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1544-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1544-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1544-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Filbert

Filbert INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1548
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HAZELNUT HAZELNUT 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1548-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1548-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1548-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1548-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Peanut

Peanut INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1552
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PEANUT Peanut 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1552-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1552-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1552-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1552-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Pecan Nut

Pecan Nut INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1556
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PECAN Pecan 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1556-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1556-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1556-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1556-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Pistachio

Pistachio INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1560
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PISTACHIO PISTACHIO 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1560-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1560-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1560-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1560-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Barley Grain

Barley Grain INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1564
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BARLEY BARLEY 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1564-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1564-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1564-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1564-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Buckwheat Grain

Buckwheat Grain INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1568
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BUCKWHEAT BUCKWHEAT 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1568-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1568-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1568-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1568-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Oat Grain

Oat Grain INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1572
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OAT 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1572-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1572-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1572-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1572-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Rice Grain

Rice Grain INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1576
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
RICE RICE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1576-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1576-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1576-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1576-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Rye Grain

Rye Grain INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1580
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
RYE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1580-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1580-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1580-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1580-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Whole Wheat Grain

Whole Wheat Grain INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1584
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
WHEAT WHEAT 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1584-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1584-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1584-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1584-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Macadamia Nut

Macadamia Nut INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1588
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MACADAMIA NUT 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1588-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1588-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1588-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1588-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Nectarine

Nectarine INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1592
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
NECTARINE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1592-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1592-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1592-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1592-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Mango

Mango INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1596
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MANGO 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1596-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1596-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1596-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1596-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Papaya

Papaya INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1600
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PAPAYA 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1600-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1600-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1600-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1600-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Leeks

Leeks INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1604
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LEEK LEEK 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1604-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1604-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1604-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1604-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Okra

Okra INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1608
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OKRA 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1608-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1608-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1608-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1608-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Parsnip

Parsnip INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1612
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PARSNIP PARSNIP 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1612-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1612-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1612-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1612-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Chick Pea

Chick Pea INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1616
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CHICKPEA CHICKPEA 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1616-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1616-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1616-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1616-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Blackeye Pea

Blackeye Pea INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1620
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BLACK-EYED PEA BLACK-EYED PEA 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1620-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1620-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1620-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1620-4 10 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Watercress

Watercress INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1624
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
WATERCRESS 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1624-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1624-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1624-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1624-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Corn Grain

Corn Grain INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1628
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CORN 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1628-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1628-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1628-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1628-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Cacao Bean

Cacao Bean INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1632
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CHOCOLATE CHOCOLATE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1632-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1632-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1632-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1632-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Coffee

Coffee INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1636
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ARABICA COFFEE BEAN Arabica Coffee Bean 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1636-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1636-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1636-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1636-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Malt

Malt INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1652
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MALT EXTRACT, BARLEY MALT EXTRACT, BARLEY 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1652-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1652-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1652-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1652-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Brewers Yeast

Brewers Yeast INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1660
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SACCHAROMYCES CEREVISIAE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1660-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1660-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1660-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1660-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Allspice

Allspice INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1664
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALLSPICE ALLSPICE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1664-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1664-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1664-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1664-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Bay Leaf

Bay Leaf INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1668
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LAURUS NOBILIS LAURUS NOBILIS 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1668-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1668-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1668-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1668-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Caraway Seed

Caraway Seed INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1672
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CARAWAY SEED CARAWAY SEED 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1672-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1672-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1672-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1672-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Cinnamon

Cinnamon INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1676
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CINNAMON 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1676-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1676-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1676-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1676-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Cloves

Cloves INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1680
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CLOVE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1680-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1680-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1680-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1680-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Dill

Dill INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1688
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DILL DILL 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1688-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1688-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1688-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1688-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Garlic

Garlic INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1692
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
GARLIC Garlic 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1692-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1692-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1692-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1692-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Ginger

Ginger INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1696
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
GINGER 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1696-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1696-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1696-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1696-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Horseradish

Horseradish INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1700
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HORSERADISH HORSERADISH 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1700-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1700-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1700-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1700-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


Licorice

Licorice INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:36987-1704
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LICORICE 0.1 g

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36987-1704-1 5 in 1 VIAL, MULTI-DOSE
2 NDC:36987-1704-2 10 in 1 VIAL, MULTI-DOSE
3 NDC:36987-1704-3 30 in 1 VIAL, MULTI-DOSE
4 NDC:36987-1704-4 50 in 1 VIAL, MULTI-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 1972-08-29


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Be sure to consult your doctor before taking any medication!
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