ROBITUSSIN CF- dextromethorphan hydrobromide, guaifenesin, pseudoephedrine hydrochloride liquid 
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC

----------

Robitussin® CF

Active ingredients (in each 5 mL tsp)Purpose

Dextromethorphan HBr, USP 10 mg

Cough suppressant

Guaifenesin, USP 100 mg

Expectorant

Pseudoephedrine HCl, USP 30 mg

Nasal decongestant

Uses

helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive
temporarily relieves these symptoms occurring with a cold:
nasal congestion
cough due to minor throat and bronchial irritation

Warnings

Do not use if you are now taking a prescription monoamine oxidase inhibitor (MAOl) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOl drug. If you do not know if your prescription drug contains an MAOl, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

heart disease
high blood pressure
thyroid disease
diabetes
trouble urinating due to an enlarged prostate gland
cough that occurs with too much phlegm (mucus)
cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema

When using this product do not use more than directed.

Stop use and ask a doctor if

you get nervous, dizzy, or sleepless
symptoms do not get better within 7 days or are accompanied by fever
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 use.

Directions

do not take more than 4 doses in any 24-hour period
agedose

adults and children 12 years and over

2 teaspoonfuls every 4 hours

children 6 years to under 12 years

1 teaspoonful every 4 hours

under 6 years

Do not use

Inactive ingredients

citric acid, FD&C red no. 40, flavors, glycerin, propylene glycol, saccharin sodium, sodium benzoate, sorbitol, water.

Keep out of reach of children. In case of overdose, get medical help right away.

Other information

store at 20-25°C (68-77°F)
dosage cup provided

MADE IN U.S.A.

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Carton

Wyeth®

Robitussin®

CF

NASAL DECONGESTANT
COUGH SUPPRESSANT
EXPECTORANT

CLEARS
NASAL STUFFINESS
CONTROLS COUGHS
LOOSENS and RELIEVES
CHEST CONGESTION

COUGH FORMULA
For Children and Adults

4 FL OZ (118 mL)

Principal Display Panel - 118 mL Bottle Carton
ROBITUSSIN CF 
dextromethorphan hydrobromide, guaifenesin, pseudoephedrine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0031-8678
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 5 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE30 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0031-8678-821 in 1 CARTON07/01/2015
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Export only07/01/2015
Labeler - GlaxoSmithKline Consumer Healthcare Holdings (US) LLC (079944263)

Revised: 1/2023
Document Id: 4c028206-cc2e-4750-bc66-588d1fe719f4
Set id: caefc641-8470-4154-98a6-c0786071414e
Version: 6
Effective Time: 20230117
 
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC