Label: WALGREENS CHILDRENS- nighttime cough liquid

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 1, 2025

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  • Active ingredients (in each 10 mL)

    Chlorpheniramine maleate, USP 2 mg

    Dextromethorphan HBr USP 15 mg

  • Purpose

    Antihistamine

    Cough suppressant

  • 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
    • itching of the nose or throat 
    • itchy, watery eyes
  • 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

    • 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

    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

    • each 10 mL contains: sodium 3 mg
    • store at room temperature. Do not refrigerate
    • contain low sodium
    • do not use if printed seal under cap is torn or missing
  • 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)

    Walgreens PHARMACIST RECOMMENDED †

    Health expertise you rely on, quality you trust

    †Walgreens Pharmacists Survey

    *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

    Walgreens

    100% SATISFACTION GUARANTEED

    Walgreens.com ©2020 Walgreen Co.

    Walgreens Childrens Nighttime Cough 188 mL
  • INGREDIENTS AND APPEARANCE
    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)
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