Presgen B description, usages, side effects, indications, overdosage, supplying and lots more!

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Presgen B

Kramer Novis
Kramer Novis

DRUG FACTS




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients/5 ml: brompheniramine maleate 4 mg, dextromethorphan hydrobromide 20 m, phenylephrine hydrochloride 10 mg

Purpose

Decongestant, antihistamine, antitussive (anti cough)

Uses

:   relieves nasal congestion associated with sinusitis. relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies. relieves sinus congestion and pressure ,helps decongest sinus openings and passages. restores free breathing. suppresses cough due to minor throat and bronchial irritation associated with a cold or inhaled irritants. relieves runny nose and reduces sneezing, itching of the nose or throat, and itchy, watery eyes due to hay fever or other upper respiratory allergie

Warnings A persistent cough may be a sign of a serious condition.  If cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache, consult a doctor

Do not: Use more than the recommended dose. Give this product to a child who has heart disease, high blood pressure, thyroid disease, or diabetes unless directed by a doctor
May cause excitability especially in children
Do not take this product, unless directed by a doctor, if you have a breathing problem such as emphysema or chronic bronchitis, or if you have glaucoma or difficulty in urination due to enlargement of the prostate gland
May cause drowsiness: alcohol, sedatives, and tranquilizers may increase the drowsiness effect.  Avoid alcoholic beverages while taking this product.  Do not take this product if you are taking sedatives or tranquilizers, without first consulting your doctor.  Use caution when driving a motor vehicle or operating machinery
when using this product do not exceed recommended dose
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 MAOI drug
. If you do not know if your prescription drug contains an MAOI, consult a doctor or pharmacist before  taking this product

Stop use and ask a doctor if:  symptoms do not improve, new symptoms occur, redness or swelling is present, nervousness, dizziness or sleeplessness occur, symptoms do not improve within 7 days or are accompanied by fever, cough persists for more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache
Ask a doctor before use if you have:  heart disease, high blood pressure, thyroid disease, diabetes, difficulty in urination due to enlargement of the prostate gland, persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema or where cough is accompanied by excessive phlegm (mucus)
In case of accidental overdose, contact a Poison Control center immediately
Prompt medical attention is critical for adults as well as children, even if you do not notice any signs or symptoms.

Keep this and all medicines out of the reach of children

As with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using this product

Inactives: Citric Acid, Flavor, Glycerin, Methylparaben, propylene Glycol, Propylparaben, Purified Water, Sodium Citrate, Sucralose

MM1

Presgen B

Adults and children 12 years of age and older-Take 1 teaspoons (5 ml) every 4 hours as needed, do not exceed 6 teaspoons in 24 hours, or as directed by a doctor

Children 6-12 years, Take 1/2 teaspoon (2.5 ml) every 4 hours as needed, do not exceed 3 teaspoons in 24 hours, or as directed by a doctor

Children under 6 years, consult a physician

Presgen B

dextromethorphan hydrobromide, brompheniramine maleate, phenylephrine hydrochloride SYRUP

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52083-637
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 20 mg
Brompheniramine Maleate BROMPHENIRAMINE 4 mg
Phenylephrine Hydrochloride PHENYLEPHRINE 10 mg

Inactive Ingredients

Ingredient Name Strength
water
CITRIC ACID MONOHYDRATE
SODIUM CITRATE
METHYLPARABEN
PROPYLPARABEN
GLYCERIN
propylene glycol
Sucralose

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52083-637-16 480 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2011-03-29


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Be sure to consult your doctor before taking any medication!
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