ROBITUSSIN TO GO COUGH AND COLD CF- dextromethorphan hbr, guaifenesin, phenylephrine hcl solution 
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.

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Robitussin To Go Cough & Cold CF
(dextromethorphan HBr, guaifenesin, and phenylephrine HCl)

DRUG FACTS

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

Dextromethorphan HBr, USP 20 mg

Guaifenesin, USP 200 mg

Phenylephrine HCl, USP 10 mg

PURPOSES

Cough suppressant

Expectorant

Nasal decongestant

USES

  • helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes
  • 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 (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

  • 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.

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 6 mg
  • store at 20-25°C (68-77°F)

INACTIVE INGREDIENTS

anhydrous citric acid, FD&C red no. 40, glycerin, menthol, natural & artificial flavor, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol solution, 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.

Adult

Robitussin To Go Cough & Cold CF

new!

DEXTROMETHORPHAN HBr (Cough Suppressant)

GUAIFENESIN (Expectorant)

PHENYLEPHRINE HCl (Nasal Decongestant)

NON-DROWSY

RELIEVES:

Cough

Stuffy Nose

Chest Congestion/Mucus

For Ages 12 & Over

Alcohol-Free

10 SINGLE DOSE PACKS

Take It Anywhere!

0.34 FL OZ. (10mL) 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 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 & Cold CF packaging
ROBITUSSIN TO GO COUGH AND COLD CF 
dextromethorphan hbr, guaifenesin, phenylephrine hcl solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0031-8713
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 10 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg  in 10 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
ColorRED (clear red liquid) Score    
ShapeSize
FlavorBERRY (berry citrus flavor) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0031-8713-1010 in 1 CARTON01/07/200809/30/2012
11 in 1 POUCH
110 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
2NDC:0031-8713-022 in 1 CARTON01/07/200809/30/2012
21 in 1 POUCH
210 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 FINALpart34101/07/200809/30/2012
Labeler - Richmond Division of Wyeth (829390835)

Revised: 10/2017
Document Id: f64967c4-01e5-40ba-af5c-6bc8013cc9a6
Set id: c4e411ab-fcb7-3c55-62d2-d89b40c4db50
Version: 6
Effective Time: 20171020
 
Richmond Division of Wyeth