Label: CHILDRENS ALLERGY DYE FREE WAL DRYL- diphenhydramine hydrochloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 25, 2025

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient (in each 5 mL)

    Diphenhydramine HCl USP 12.5 mg

  • Purpose

    Antihistamine

  • Uses

    • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
      • runny nose
      • sneezing
      • itchy, watery eyes
      • itching of the throat or nose
  • Warnings

    Do not use

    • to make a child sleepy
    • with any other product containing diphenhydramine, even one used on skin

    Ask a doctor before use if the child has

    • a breathing problem such as chronic bronchitis
    • glaucoma

    Ask a doctor or pharmacist before use if the child istaking sedatives or tranquilizers

    When using this product

    • marked drowsiness may occur
    • sedatives and tranquilizers may increase drowsiness
    • excitability may occur, especially in children

    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

    • find right dose on chart below
    • take every 4 to 6 hours, or as directed by a doctor
    • do not take more than 6 doses in 24 hours
    • mL = milliliter

    Age (yr)

    Dose (mL)

    children under 2 years

    do not use

    children 2 to 5 years

    do not use unless directed by a doctor

    children 6 to 11 years

    5 mL to 10 mL

    Attention:use only enclosed dosing cup designed for use with this product. Do not use any other dosing device

  • Other information

    • each 5 mL contains: sodium 11 mg
    • store at room temperature
    • see bottom panel for lot number and expiration date
    • protect from light
    • contains very low sodium
  • Inactive ingredients

    anhydrous citric acid, carboxymethylcellulose sodium, flavors, glycerin, potassium citrate, purified water, sodium benzoate, sorbitol, sucralose.

    Questions?

    1-866-467-2748

  • PRINCIPAL DISPLAY PANEL

    Walgreens

    NDC 0363-0710-08

    Compare to Children’s Benadryl ®Dye-Free active ingredient††

    children’s ALLERGY Dye-Free Wal-Dryl®

    DIPHENHYDRAMINE HCl /ANTIHISTAMINE

    12.5 mg/ 5 mL ORAL SOLUTION

    DYE & SUGAR FREE

    • For the relief of runny nose, itchy throat or nose, sneezing, & itchy, watery eyes
    • AGES 6 -11 YEARS

    BUBBLE GUM FLAVOR

    8 FL OZ (236 mL)

    Walgreens

    Pharmacist Recommended†

    Health expertise you rely on, quality you trust.

    †Walgreens Pharmacist Survey

    ††This product is not manufactured or distributed by Johnson and Johnson owner of the registered trademark Children’s Benadryl ®Dye–Free

    DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS TORN OR MISSING

    IMPORTANT : KEEP THIS CARTON FOR FUTURE REFERENCE ON FULL LABELING

    DISTRIBUTED BY: WALGREEN CO.

    200 WILMOT RD.,DEERFIELD,IL 60015

    Walgreens

    100% SATISFACTION GUARANTEED

    walgreens.com ©2017 Walgreen Co.

    Children's Allergy Dye- Free Wal - Dryl BUBBLE GUM FLAVOR 8 FL OZ (236 mL)
  • INGREDIENTS AND APPEARANCE
    CHILDRENS ALLERGY DYE FREE WAL DRYL 
    diphenhydramine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0710
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE12.5 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM CITRATE (UNII: EE90ONI6FF)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorBUBBLE GUMImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0710-081 in 1 CARTON08/31/2017
    1236 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01208/31/2017
    Labeler - WALGREEN CO. (008965063)
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