Wal-Tussin DM by Walgreen Company / AptaPharma Inc. Wal-Tussin® DM

Wal-Tussin DM by

Drug Labeling and Warnings

Wal-Tussin DM by is a Otc medication manufactured, distributed, or labeled by Walgreen Company, AptaPharma Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WAL-TUSSIN DM- dextromethorphan hbr, guaifenesin liquid 
Walgreen Company

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.

----------

Wal-Tussin® DM

Drug Facts

Active ingredients (in each 10 mL)
Dextromethorphan HBr, USP 20 mg
Guaifenesin, USP 200 mg

Purpose
Dextromethorphan HBr, USP .......................Cough Suppressant
Guaifenesin, USP ....................................... 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 tube

Warnings

Do not use ■ in a child under 12 years of age
■ 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 adoctor 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

                Age                Dose
 adults & children 12 years & over    10 mL every 4 hours
 children under 12 years             do not use

Other information
Keep carton for full Direction for use.
■ store at 20-25°C (68-77°F)
■ do not refrigerate
■ dosage cup provided
■ sodium 6 mg per 10 mL

Inactive ingredients
anhydrous citric acid, dextrose, FD&C red # 40, flavor, glycerin, high fructose corn syrup,
menthol, purified water, saccharin sodium, sodium benzoate.

Questions? Call weekdays from 9:30 AM to 4:30 PM EST at 1-877-798-5944.

Product Label

Walgreens

Compare to Robitussin® Peak
Cold Cough & Chest Congestion
DM active ingredients††

                         NDC: 0363-0324-28

ADULT NON-DROWSY
Wal-Tussin®
DM

COUGH & CHEST
CONGESTION

DEXTROMETHORPHAN HBr /
COUGH SUPPRESSANT
GUAIFENESIN / EXPECTORANT

ALCOHOL FREE

Relieves cough &
   chest congestion
12 years & older

12 FL OZ (354 mL)

ORG1020-F2

DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING

Walgreens Pharmacist Survey
††This product is not manufactured or distributed by PF Consumer Healthcare1
LLC, owner of the registered trademark Robitussin® Peak Cold.

DISTRIBUTED BY WALGREEN CO.
200 WILMONT RD., DEERFIELD, IL 60015

Walgreens
100% SATISFACTION
           GUARANTEED

walgreens.com ©2020 Walgreen Co.

DOSAGE
CUP PROVIDED
             BX-112

Carton

WalTussin DM Box

Bottle

WalTussin DM Btl

res

WAL-TUSSIN DM 
dextromethorphan hbr, guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 0363-0324
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
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
DEXTROSE (UNII: IY9XDZ35W2)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
MENTHOL (UNII: L7T10EIP3A)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Product Characteristics
ColorredScore    
ShapeSize
FlavorFRUIT PUNCHImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 0363-0324-281 in 1 CARTON11/13/2020
1354 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34111/13/202012/01/2022
Labeler - Walgreen Company (008965063)
Registrant - AptaPharma Inc. (790523323)
Establishment
NameAddressID/FEIBusiness Operations
AptaPharma Inc.790523323manufacture(0363-0324)

Revised: 12/2022
 

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.