WALGREENS CHILDRENS- nighttime cough liquid 
WALGREENS CO.

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Walgreens Children’s Night-Time Cough & Chest Congestion

Active ingredients (in each 10 mL)

Chlorpheniramine maleate, USP 2 mg

Dextromethorphan HBr USP 15 mg

Purpose

Antihistamine

Cough suppressant

Uses

Warnings

Do not us

  • 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 enlarges 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.
  • 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 last 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 (1-800-222-1222) right away

Directions

age

dose

Children under 6 years

Do not use

Children 6 to under 12 years

10 mL every 6 hours

Adults and children 12 years and older

20 mL every 6 hours

Other information

Inactive ingredients

anhydrous citric acid, FD&C Red # 40, flavor, potassium sorbate, potassium citrate, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose

Questions or comments?

1-866-467-2748

Principal Display Panel

Compare to the Children's Robitussin ®Nighttime Cough DM active ingredients ††

NDC# 0363-7560-04

Children's

Nighttime Cough

Wal-Tussin ®DM

CHLORPHENIRAMINE MALEATE, USP 2 mg/10 mL

ANTIHISTAMINE

DEXTROMETHORPHAN HBr, USP 15 mg/15 mL

COUGH SUPPRESSANT

NIGHTTIME

Relieves cough & runny nose

6 YEARS & OLDER

Fruit Punch Flavor

NATURALLY AND ARTIFICIALLY FLAVORED

Dosage cup included

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

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*This product is not manufactured or distributed by Pfizer, owner of the registered trademarks Children’s Robitussin ®

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

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Walgreens Childrens Nighttime Cough 188 mL
WALGREENS CHILDRENS 
nighttime cough liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-7560
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE2 mg  in 10 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
ColorredScore    
ShapeSize
FlavorFRUIT PUNCHImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-7560-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product07/16/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01007/16/2019
Labeler - WALGREENS CO. (008965063)

Revised: 12/2025
Document Id: 44e1c78e-5a2e-a020-e063-6394a90ab73a
Set id: a270cbe3-bf0a-44da-9359-00e218eba239
Version: 7
Effective Time: 20251201
 
WALGREENS CO.