ROBITUSSIN CHEST CONGESTION- guaifenesin liquid

ROBITUSSIN CHEST CONGESTION by

Drug Labeling and Warnings

ROBITUSSIN CHEST CONGESTION by is a Otc medication manufactured, distributed, or labeled by Wyeth Consumer Healthcare LLC, Pfizer Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 Carton

Robitussin®

(GUAIFENESIN
SYRUP, USP)

EXPECTORANT

• LOOSENS and RELIEVES
  CHEST CONGESTION

ALCOHOL-FREE
COUGH FORMULA
For Children and Adults

4 FL OZ (118 mL)

PRINCIPAL DISPLAY PANEL - Leaflet

INGREDIENTS AND APPEARANCE

ROBITUSSIN CHEST CONGESTION 
guaifenesin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0031-8748
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	100 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
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
Color	RED	Score
Shape		Size
Flavor	RASPBERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0031-8748-04	1 in 1 CARTON	09/09/2013
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
EXPORT ONLY		09/21/2004

Labeler - Wyeth Consumer Healthcare LLC (828831730)

Registrant - Pfizer Inc (113480771)