ROBITUSSIN LINGERING COLD LONG-ACTING COUGHGELS- dextromethorphan hbr capsule, liquid filled 
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC

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 Lingering Cold Long-Acting CoughGels
(dextromethorphan HBr)

DRUG FACTS

ACTIVE INGREDIENT (IN EACH LIQUID-FILLED CAPSULE)

Dextromethorphan HBr, USP 15 mg

PURPOSE

Cough suppressant

USE

temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold.

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

a cough that occurs with too much phlegm (mucus)
a cough that lasts or is chronic as occurs with smoking, asthma, 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 8 capsules 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 over

take 2 capsules every 6 to 8 hours, as needed

children under 12 years

do not use

OTHER INFORMATION

store at 20-25°C (68-77°F)
avoid excessive heat above 40°C (104°F)
protect from light

INACTIVE INGREDIENTS

FD&C blue no. 1, FD&C red no. 40, fractionated coconut oil, gelatin, glycerin, mannitol, pharmaceutical ink, polyethylene glycol, povidone, propyl gallate, propylene glycol, purified water, sorbitol, sorbitol anhydrides

QUESTIONS OR COMMENTS?

Call weekdays from 9 AM-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 LINGERING COLD Long-Acting CoughGels

DEXTROMETHORPHAN HBr (Cough Suppressant)

Relieves: Cough for up to 8 Hours

Non-Narcotic Formula

Non-Drowsy

For Ages 12 & Over

20 LIQUI-GELS*

*Liquid-Filled Capsules

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

Stop use and ask a doctor if cough lasts more than 7 days.

Pfizer, Madison, NJ 07940 USA © 2011 Pfizer Inc.

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

LIQUI-GELS is a trademark or registered trademark of Catalent Pharma Solutions.

Robitussin Lingering Cold Long-Acting CoughGels Packaging
ROBITUSSIN LINGERING COLD LONG-ACTING COUGHGELS 
dextromethorphan hbr capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0031-8741
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 (UNII: WZB9127XOA)  
COCONUT OIL (UNII: Q9L0O73W7L)  
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
MANNITOL (UNII: 3OWL53L36A)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
PROPYL GALLATE (UNII: 8D4SNN7V92)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
Product Characteristics
ColorRED (clear red) Scoreno score
ShapeOVAL (oval softgel) Size10mm
FlavorImprint Code R
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0031-8741-201 in 1 BLISTER PACK06/06/201106/01/2022
120 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34106/06/201106/01/2022
Labeler - GlaxoSmithKline Consumer Healthcare Holdings (US) LLC (079944263)
Establishment
NameAddressID/FEIBusiness Operations
PF Consumer Healthcare Canada ULC203812479ANALYSIS(0031-8741) , LABEL(0031-8741) , PACK(0031-8741)

Revised: 1/2021
 
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC