Wal-Tussin DM

Manufacturer: Walgreen Company | AptaPharma Inc.
Effective date: 2020-11-25
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:05:31

Label at a glance#

ProductWal-Tussin DM

Active ingredientDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN

Label structure14 sections

Contacts and useful links#

PhoneLabel contact1-877-798-5944

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

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

INDICATIONS & USAGE SECTION

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 SECTION

Warnings

OTC - DO NOT USE SECTION

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.

OTC - ASK DOCTOR SECTION

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

OTC - STOP USE SECTION

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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

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 SAFETY INFORMATION

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 INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

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

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

DOSAGE
CUP PROVIDED
BX-112

Carton

WalTussin DM Box

Bottle

WalTussin DM Btl

res

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

Wal-Tussin DM
DEXTROMETHORPHAN HBr, GUAIFENESIN
DEXTROMETHORPHAN HYDROBROMIDE
DEXTROMETHORPHAN
GUAIFENESIN
ANHYDROUS CITRIC ACID
DEXTROSE
FD&C RED NO. 40
GLYCERIN
HIGH FRUCTOSE CORN SYRUP
MENTHOL
WATER
SACCHARIN SODIUM
SODIUM BENZOATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0363-0324	0363-0324-28

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DEXTROMETHORPHAN HYDROBROMIDE	9D2RTI9KYH	ACTIB
GUAIFENESIN	495W7451VQ	ACTIB
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT
DEXTROSE	IY9XDZ35W2	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
GLYCERIN	PDC6A3C0OX	IACT
HIGH FRUCTOSE CORN SYRUP	XY6UN3QB6S	IACT
MENTHOL	L7T10EIP3A	IACT
WATER	059QF0KO0R	IACT
SACCHARIN SODIUM	SB8ZUX40TY	IACT
SODIUM BENZOATE	OJ245FE5EU	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
13689c3f-713f-43bf-8450-76db37ea8d07			054b44e8-0226-4cbd-a113-13da0ac90f05	2022-12-16	Warnings	Exact identifier spl set id: 054b44e8-0226-4cbd-a113-13da0ac90f05

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.