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ConRx

Eagle Distributors,Inc.

ConRx Allergy Sinus Multi-Symptoms


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient (in each tablet)

Acetaminophen 325mg

Chlorpheniramine maleate 2mg

Phenylephrine HCl 5mg

Purpose

Pain reliever/ fever reducer

Antihistamine

Nasal decongestant

ConRx Uses

Uses For the temporary relieves these symptoms of hay fever or other upper respiratory allergies, headache, sinus congestion and pressure, nasal congestion, runny nose and sneezing ,minor aches and pains, itching of the nose or throat ,itchy watery eyes, help decongest sinus openings and passages.

Warnings

  • Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take: more than 8 tablets in 24 hours, which is the maximum daily amount for this product
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product

Do not use

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
  • If you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use if you have

  • liver disease
  • heart disease
  • high blood pressure
  • thyroid disease
  • diabetes
  • trouble urinating due to an enlarged prostate gland
  • a breathing problem such as emphysema or chronic bronchitis,
  • glaucoma

Ask a doctor or pharmacist before use if you are taking

  • the blood thinning drug warfarin

When using this product

  • do not exceed recommended dosage
  • excitability may occur, especially in children
  • drowsiness may occur
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • avoid alcoholic drinks
  • be careful when driving a motor vehicle or operating machinery

Stop use and ask a doctor if

  • nervousness, dizziness, or sleeplessness occur
  • pain or nasal congestion gets worse or lasts more than 7 days
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present
  • new symptoms occur

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

Overdose warning

In case of overdose, get medical help or contact a Poison Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

Do not taking more than directed (see overdose warning)

Adults and Children 12 years and above
  • Take 1-2 tablets every 4 hours
  • Do not taking more than 8 tablets in 24 hour
Children under 12 years of age Consult a doctor

Other Information

  • Do not use if pouch is torn or damaged.
  • Store between 15-30°C (59-86°F). Avoid excessive heat and humidity.
  • See side panel for lot number and expiration date.

Inactive ingredients

Colloidal silicon dioxide, Sodium Lauryl Sulphate, Edetaet disodium, Dioctyl Sodium Sulphosuccinate, Polyvinylpyrollidone, Gelatin, Corn starch', Magnesium Stearate, Microcrystalline Cellulose, Polyethylene glycol 6000,Sodium Benzoate ,Sodium Starch Glycolate, Stearic acid, Purified Talc, Titanium Dioxide, Yellow iron oxide.

PRINCIPAL DISPLAY PANEL - 50 Pouch Carton

NDC:68737-225-09

Compare to the Active Ingredients in
Tylenol ® Allergy
Multi-Symptom*

ConRx
Allergy MULTI - SYMPTOM
Sinus

Sneezing - Runny Nose - Congestion

 

  • Acetaminophen                      Headache
  • Phenylephrine HCl                    Sinus Pressure/Nasal Congestion
  • Chlorpheniramine Maleate       Watery Eyes/Runny Nose
ConRx

ConRx

Acetaminophen, Chlorpheniramine maleate, and Phenylephrine Hydrochloride TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68737-225
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ACETAMINOPHEN ACETAMINOPHEN 325 mg
Chlorpheniramine Maleate CHLORPHENIRAMINE 2 mg
Phenylephrine Hydrochloride PHENYLEPHRINE 5 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
SODIUM LAURYL SULFATE
EDETATE DISODIUM
BIS(1-METHYLAMYL) SODIUM SULFOSUCCINATE
POVIDONE K90
GELATIN
STARCH, CORN
MAGNESIUM STEARATE
cellulose, microcrystalline
polyethylene glycol 6000
SODIUM BENZOATE
sodium starch glycolate type a corn
STEARIC ACID
talc
titanium dioxide
FERRIC OXIDE YELLOW

Product Characteristics

Color Size Shape
WHITE 12 mm ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 2 in 1 POUCH
2 NDC:68737-225-09 50 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2012-07-11


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Be sure to consult your doctor before taking any medication!
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