Supress DM description, usages, side effects, indications, overdosage, supplying and lots more!

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Supress DM

Kramer Novis
Kramer Novis

DRUG FACTS




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients in each 1 ml: Guaifenesin 50 mg, dextromethorphan hydrobromide 5 mg

Purpose

Cough Suppressant, Expectorant

Uses

suppresses cough due to minor throat and bronchial irritation associated with
a cold or inhaled irritants
• helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial
passages of bothersome mucus, drain bronchial tubes, and make coughs
more productive

Warnings Do not use if if a child is 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.

Ask a doctor before use for: A cough that occurs with too much phlegm (mucus)-Cough that lasts or is chronic such as occurs with asthma

Stop use and ask a doctor if: new symptoms occur•symptoms do not get better within 7 days or are accompanied by fever
•coughs lasts more than 7 days, comes back, or is accompanied by fever,
rash, or a persistent headache. These could be signs of a serious condition


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, Cherry FlavorFlavor, Glycerin, Methyl Paraben, Potassium Sorbate, Propyl
Paraben, Propylene Glycol, Purified Water, Sodium Citrate, Sodium Saccharin.

MM1

Supress DM

Children 2-6 years, 1 mL every 4 hours as needed, Do not exceed 6 doses in any 24-hour, or as directed by a doctor

Children under 2 years, consult a doctor

neasure with the dosage device provided.  Do not use with any other device.

Supress DM

dextromethorphan hydrobromide, guaifenesin SYRUP

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52083-058
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Guaifenesin GUAIFENESIN 50 mg
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 5 mg

Inactive Ingredients

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

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52083-058-01 30 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2013-10-02


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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