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WalTussin DM Max

Dosage form: kit
Ingredients: DEXTROMETHORPHAN HYDROBROMIDE 20mg in 10mL, GUAIFENESIN 400mg in 10mL; DEXTROMETHORPHAN HYDROBROMIDE 30mg in 10mL, DOXYLAMINE SUCCINATE 12.5mg in 10mL
Labeler: Walgreen Company
NDC Code: 0363-0918

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.

Walgreen Co. Wal-Tussin® DM Max Nighttime Wal-Tussin® DM Max Drug Facts

Nighttime Cough DM
Active ingredients (in each 10 mL)

Dextromethorphan HBr, USP 30 mg

Doxylamine succinate, USP 12.5 mg

Purposes

Cough suppressant

Antihistamine

Uses
temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
runny nose
sneezing
itchy, watery eyes
itching of the nose or throat
controls the impulse to cough to help you sleep

Warnings

Do not use - Daytime
to make a child sleepy
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
trouble urinating due to an enlarged prostate gland
glaucoma
cough that occurs with too much phlegm (mucus)
a breathing problem such as emphysema or chronic bronchitis
persistent or chronic cough such as occurs with smoking, asthma, or emphysema

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers

When using this product
do not use more than directed
marked drowsiness may occur
avoid alcoholic drinks
alcohol, sedatives, and tranquilizers may increase drowsiness
be careful when driving a motor vehicle or operating machinery
excitability may occur, especially in children

Stop use and ask a doctor if

cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign 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 (1-800-222-1222).

Directions
measure only with dosing cup provided
keep dosing cup with product
mL = milliliter
do not take more than 4 doses in any 24-hour period
this adult product is not intended for use in children under 12 years of age

age

dose

adults and children

12 years and over

10 mL

every 6 hours

children under 12 years

do not use

Other information
each 10 mL contains: sodium 8 mg
store at 20-25°C (68-77°F)

Inactive ingredients

anhydrous citric acid, FD&C red #40, flavor, glycerin, high fructose corn syrup, menthol, propylene glycol, purified water, sodium benzoate, sodium citrate, sucralose, xanthan gum

Questions or comments?

1-800-719-9260

Daytime Cough + Chest Congestion DM
Active ingredients (in each 10 mL)

Dextromethorphan HBr, USP 20 mg

Guaifenesin, USP 400 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 for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign or 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 (1-800-222-1222).

Directions
shake well before using
do not take more than 6 doses in any 24-hour period
measure only with dosing cup provided
keep dosing cup with product
mL = milliliter
this adult product is not intended for use in children under 12 years of age

age

dose

adults and children

12 years and over

10 mL

every 4 hours

children under 12 years

do not use

Other information
each 10 mL contains: sodium 7 mg
store at 20-25°C (68-77°F). Do not refrigerate.

Inactive ingredients

anhydrous citric acid, D&C red no. 33, FD&C red no. 40, flavor, glycerin, high fructose corn syrup, menthol, microcrystalline cellulose and carboxymethylcellulose sodium, polyethylene glycol, povidone, propylene glycol, purified water, saccharin sodium, sodium benzoate, sorbitol solution, xanthan gum

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel

COMBO PACK

MAXIMUM STRENGTH

ADULT – NON-DROWSY

Wal-Tussin® DM Max

DM MAX

Cough & Chest Congestion

Dextromethorphan HBr / Cough Suppressant

Guaifenesin / Expectorant

Relieves cough & chest congestion / mucus

For maximum strength mucus relief

Ages 12 & older

Alcohol free

DAYTIME

CHERRY & MENTHOL FLAVOR

MAXIMUM STRENGTH

ADULT

Nighttime Wal-Tussin® DM Max

DM MAX

Cough

Dextromethorphan HBr / Cough Suppressant

Doxylamine Succinate / Antihistamine

Relieves cough, itchy throat & runny nose

Ages 12 & older

NIGHTTIME

Compare to Robitussin® Maximum Strength Cough + Chest Congestion DM and Robitussin® Maximum Strength Nighttime Cough DM active ingredients

TOTAL 8 FL OZ (236 mL) – 2 x 4 FL OZ (118 mL)

WALTUSSIN DM MAX 
dextromethorphan hbr, doxylamine succinate, guaifenesin kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0918
Packaging
#Item CodePackage Description
1NDC:0363-0918-121 KIT in 1 KIT
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE 118 mL
Part 21 BOTTLE 118 mL
Part 1 of 2
WAL TUSSIN DM MAX 
dextromethorphan hbr, guaifenesin solution
Product Information
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 10 mL
GUAIFENESIN (GUAIFENESIN) GUAIFENESIN400 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID 
D&C RED NO. 33 
FD&C RED NO. 40 
GLYCERIN 
HIGH FRUCTOSE CORN SYRUP 
MENTHOL, UNSPECIFIED FORM 
CELLULOSE, MICROCRYSTALLINE 
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM 
POLYETHYLENE GLYCOLS 
POVIDONES 
PROPYLENE GLYCOL 
WATER 
SACCHARIN SODIUM 
SODIUM BENZOATE 
SORBITOL 
XANTHAN GUM 
Product Characteristics
ColorRED (Opaque) Score    
ShapeSize
FlavorCHERRY (menthol) Imprint Code
Contains    
Packaging
#Item CodePackage Description
1118 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34110/31/2014
Part 2 of 2
NIGHTTIME WAL TUSSIN DM MAX 
dextromethorphan hbr, doxylamine succinate solution
Product Information
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE30 mg  in 10 mL
DOXYLAMINE SUCCINATE (DOXYLAMINE) DOXYLAMINE SUCCINATE12.5 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID 
FD&C RED NO. 40 
HIGH FRUCTOSE CORN SYRUP 
MENTHOL, UNSPECIFIED FORM 
PROPYLENE GLYCOL 
WATER 
SODIUM BENZOATE 
SODIUM CITRATE, UNSPECIFIED FORM 
SUCRALOSE 
XANTHAN GUM 
GLYCERIN 
Product Characteristics
ColorRED (clear) Score    
ShapeSize
FlavorFRUITImprint Code
Contains    
Packaging
#Item CodePackage Description
1118 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34107/10/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34107/10/2016
Labeler - Walgreen Company (008965063)

 
Walgreen Company

Medically reviewed on Feb 7, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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