Label: EXTRA STRENGTH WAL-DRYL ITCH RELIEF- diphenhydramine, zinc acetate spray

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

Drug Label Information

Updated December 27, 2023

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  • ACTIVE INGREDIENT

    Active Ingredients:

    Diphenhydramine HCL 2.0%      Topical Analgesic

    Zinc Acetate 0.1%         Skin Protectant

  • PURPOSE

    Purpose

    Topical Analgesic, Skin protectant.

  • INDICATIONS & USAGE

    Uses:

    Temporarily relieves pain and itching associated with:

    insect bites, minor burns and cuts, sunburn, scrapes, minor skin irritations, rashes due to poison ivy, oak and sumac, dries the oozing and weeping of poison ivy, poison oak and poison sumac.

  • WARNINGS

    Warnings:

    For external use only.

    flammable: do not use while smokingo r near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120degrees F.


  • Do not use

    On large areas of the body.
    with any other product containing diphenhydramine, even one taken by mouth.

  • ASK DOCTOR

    Ask a doctor before use

    on chicken pox

    on measles

  • WHEN USING

    When using this product, keep out of eyes, use only as directed.

  • STOP USE

    Stop use and ask doctor if:

    condition worsens

    symptoms last more than 7 days

    symptoms clear up and occur again in a few days.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


  • DOSAGE & ADMINISTRATION

    Directions

    Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily

    children under 2 years of age: ask a doctor.

  • STORAGE AND HANDLING

    Other Information

    store between 20 and 25 degrees C (68 to 77 degrees F)


  • INACTIVE INGREDIENT

    Inactive Ingredients

    Aloe barbadensis leaf juice, glycerin, purified water, sd alcohol 40-B, tromethamine

  • QUESTIONS

    Call 1-866-964-0939

  • DESCRIPTION

    *This product is not manufactured or distributed by Johnson and Johnson consumer Products company, owner of the Registered trademark Benadryl

    Distributed by Walgreen Co.

    200 Wilmot Rd., Deerfield, IL 60015-4616

    100% Satisfaction Guaranteed www.walgreens.com

    MADE IN USA

  • PRINCIPAL DISPLAY PANEL

    Compare to Benadryl(r) Spray

    Active ingredients



    Walgreens

    Extra Strength

    Wal-Dryl

    Itch Relief

    Continuous Spray

    Diphenhydramine Hydrochloride 2%

    Zinc Acetate 0.1%

    Histamine Blocking

    Topical Analgesic

    Skin Protectant



    Relieves itching and pain from insect bites, rashes, poison ivy, sumac and oak.

    3 fl oz (88mL)

  • PRINCIPAL DISPLAY PANEL

    Wal-Dryl spray

  • INGREDIENTS AND APPEARANCE
    EXTRA STRENGTH WAL-DRYL ITCH RELIEF 
    diphenhydramine, zinc acetate spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-2177
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 mL
    ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    TROMETHAMINE (UNII: 023C2WHX2V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-2177-0088 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/03/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/03/2011
    Labeler - WALGREEN CO (008965063)
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