COUGH BE GONE description, usages, side effects, indications, overdosage, supplying and lots more!

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COUGH BE GONE

RFX Pharmaceutical Co., Ltd.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in 10 ml)

Dextromethorphan Hydrobromide 20 mg

Guaifenesin USP 200 mg

Purpose

Cough suppressant

Expectorant

■ temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold ■ helps loosen phlegm (mucus) and thin bronchial secretions make coughs more productive

Do not use 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.

Ask a doctor before use if you have

■cough that occurs with too much phlegm (mucus)

■cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema

Stop use and ask a doctor if

if cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

If pregnant or breast-feeding

ask a health professional before

Keep out of reach of children

In case of overdose, get medical help or contact a Poison Control Center right away.

■do not take more than 6 doses in any 24-hour period

■one dose is one bottle

■this adult product is not intended for use in children under 12 years of age

Age                                                  Dose

adults and children 12 years           one bottle (10 ml) every 4 hours

               and over

children under 12 years                  do not use

Almond oil, Citrus peel, Ginger, Honey, Loquat leaf extract, Licorice, Menthol, Purified water

Package Label

COUGH BE GONE

COUGH BE GONE

Dextromethorphan Hydrobromide Guaifenesin LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:76206-001
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 20 mg
Guaifenesin GUAIFENESIN 200 mg

Inactive Ingredients

Ingredient Name Strength
ALMOND OIL
GINGER
HONEY
ERIOBOTRYA JAPONICA LEAF
LICORICE
MENTHOL
water

Product Characteristics

Color
brown (light brown )

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:76206-001-10 10 in 1 BOTTLE, GLASS
2 NDC:76206-001-01 6 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2014-01-30


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Be sure to consult your doctor before taking any medication!
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