ROBITUSSIN CHEST CONGESTION- guaifenesin liquid 
Wyeth Consumer Healthcare LLC

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ROBITUSSIN® CHEST CONGESTION

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label

4 FL OZ (118mL)

Robitussin®

(GUAIFENESIN SYRUP, USP)

EXPECTORANT

DIRECTIONS: Follow dosage below:
Do Not Exceed Recommended Dosage.

ADULT DOSE (and children 12 years and
over): 2 - 4 teaspoonfuls every 4 hours.

CHILD DOSE
6 yrs. to under 12 yrs.:
1 - 2 teaspoonfuls every 4 hours.

Children under 6 yrs.:
Do not use.

TAMPER-EVIDENT BOTTLE CAP.
IF BREAKABLE RING IS
SEPARATED, DO NOT USE.

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Carton

Robitussin®

(GUAIFENESIN
SYRUP, USP)

EXPECTORANT

ALCOHOL-FREE
COUGH FORMULA
For Children and Adults

4 FL OZ (118 mL)

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Carton

PRINCIPAL DISPLAY PANEL - Leaflet

PRINCIPAL DISPLAY PANEL - Leaflet
ROBITUSSIN CHEST CONGESTION 
guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0031-8748
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
CARAMEL (UNII: T9D99G2B1R)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorREDScore    
ShapeSize
FlavorRASPBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0031-8748-041 in 1 CARTON09/09/2013
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
EXPORT ONLY09/21/2004
Labeler - Wyeth Consumer Healthcare LLC (828831730)
Registrant - Pfizer Inc (113480771)

Revised: 12/2019
Document Id: f7b7c076-0f82-44df-a0b9-11b60a6679c1
Set id: 94455035-2482-4b27-8870-45b9b7335696
Version: 2
Effective Time: 20191204
 
Wyeth Consumer Healthcare LLC