ROBITUSSIN TO GO COUGH AND CHEST CONGESTION DM- dextromethorphan hbr, guaifenesin liquid 
Richmond Division of Wyeth

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Robitussin To Go Cough & Chest Congestion DM
(dextromethorphan HBr and guaifenesin)

DRUG FACTS

ACTIVE INGREDIENTS (IN EACH 10 ML PRE-FILLED SPOON)

Dextromethorphan HBr, USP 20 mg

Guaifenesin, USP 200 mg

PURPOSES

Cough suppressant

Expectorant

USES

  • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
  • helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes

WARNINGS

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

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.

Keep out of reach of children.

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

DIRECTIONS

  • do not take more than 6 doses in any 24-hour period
  • this adult product is not intended for use in children under 12 years of age
agedose
adults and children 12 years and over1 pre-filled spoon every 4 hours
children under 12 yearsdo not use

OTHER INFORMATION

  • each pre-filled spoon contains: sodium 14 mg
  • store at 20-25°C (68-77°F)

INACTIVE INGREDIENTS

anhydrous citric acid, FD&C red no. 40, glycerin, high fructose corn syrup, menthol, natural flavor, propylene glycol, purified water, sodium benzoate, sodium citrate, sucralose

QUESTIONS OR COMMENTS?

call weekdays from 9 AM to 5 PM EST at 1-800-762-4675

PRODUCT PACKAGING

The product packaging shown below represents a sample of that currently in use. Additional packaging may also be available.

new!

Adult

Robitussin To Go Cough & Chest Congestion DM

Dextromethorphan HBr (Cough Suppressant)

Guaifenesin (Expectorant)

NON-DROWSY

RELIEVES:

Cough

Chest Congestion/Mucus

For Ages 12 & Over

Alcohol-Free

10 SINGLE DOSE PACKS

Take It Anywhere!

0.34 FL OZ. (10 mL) EACH

WARNING: CHOKING HAZARD - - Small Parts. Keep out of reach of small children.

DIRECTIONS:

1 Fold along dotted line and tear at slit to remove container or use scissors

2 Twist off cap

3 Place spoon end of container in mouth

4 Squeeze firmly to deliver medication

Carton contains individual pouches. Do Not Use if pouch seal is torn or broken. Spoon is not child resistant. Do not remove spoon from child resistant foil pouch prior to use. Discard after use.

U.S. Patent D534, 648. Other patents pending.

Wyeth Consumer Healthcare, Madison, NJ 07940 USA ©2008 Wyeth

For most recent product information, visit www.robitussin.com

PARENTS: Learn about teen medicine abuse www.StopMedicineAbuse.org

Rite Dose SQUEEZE IT'S INSIDE

Robitussin To Go Cough and Chest Congestion DM Packaging
ROBITUSSIN TO GO COUGH AND CHEST CONGESTION DM 
dextromethorphan hbr, guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0031-8712
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE2 mg  in 1 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
ColorRED (clear red liquid) Score    
ShapeSize
FlavorPINEAPPLE (pineapple orange flavor) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0031-8712-1010 in 1 BOX07/31/200708/31/2012
110 in 1 POUCH
110 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34107/31/200708/31/2012
Labeler - Richmond Division of Wyeth (829390835)

Revised: 2/2019
Document Id: dae41f26-e815-4e3f-a2a2-f954eed3a9db
Set id: 7c2138fd-bb20-3356-1e45-d8756e47f2cc
Version: 7
Effective Time: 20190220
 
Richmond Division of Wyeth