WALGREENS ADULT NIGHTTIME WAL TUSSIN DM MAX MAXIMUM STRENGTH- dextromethorphan hbr, doxylamine succinate solution

Walgreens Adult Nighttime Wal Tussin DM Max Maximum Strength by

Drug Labeling and Warnings

Walgreens Adult Nighttime Wal Tussin DM Max Maximum Strength by is a Otc medication manufactured, distributed, or labeled by WALGREEN CO.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients (in each 20 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

• to sedate a child or 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
• a cough that occurs with too much phlegm (mucus)
• a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis 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

• 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 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 at 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:

  20 mL every 6 hours

• children under 12 years:

  do not use

Other information:

• each 20mL contains: sodium 4 mg
• store at room temperature

Inactive ingredients

anhydrous citric acid, FD&C red no. 40, flavors, menthol, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum.

Questions or comments?

1-866-467-2748

DO NOT USE IF INNER SEAL IS BROKEN OR MISSING

Principal Display Panel

Walgreens

Compare to Robitussin® Maximum Strength Nighttime Cough DM active ingredients‡

NDC: 0363-0758-04

ADULT

Nighttime

Wal-Tussin®

DM Max

COUGH

DEXTROMETHORPHAN HBr 30 mg / COUGH SUPPRESSANT

DOXYLAMINE SUCCINATE 12.5 mg / ANTIHISTAMINE

MAXIMUM STRENGTH

• Relieves cough, itchy throat & runny nose
• 12 Years & older

‡Walgreens Pharmacist Survey

WALGREENS PHARMACIST RECOMMENDED‡

‡‡This product is not manufactured or distributed by Pfizer distributor of Robitussin® Maximum Strength Nighttime Cough DM

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD.,DEERFIELD,IL 60015

Walgreens 100% SATISFACTION GUARANTEED

Walgreens.com ©2017 Walgreen Co.

4 FL OZ (118 mL)

INGREDIENTS AND APPEARANCE

WALGREENS ADULT NIGHTTIME WAL TUSSIN DM MAX MAXIMUM STRENGTH 
dextromethorphan hbr, doxylamine succinate solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0758
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	30 mg  in 20 mL
DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL)	DOXYLAMINE SUCCINATE	12.5 mg  in 20 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
FD&C RED NO. 40 (UNII: WZB9127XOA)
MENTHOL (UNII: L7T10EIP3A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SORBITOL (UNII: 506T60A25R)
SUCRALOSE (UNII: 96K6UQ3ZD4)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	RED	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0758-04	1 in 1 CARTON	09/08/2017
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	09/08/2017

Labeler - WALGREEN CO. (008965063)