Label: WAL-DRYL- diphenhydramine hydrochloride and zinc acetate cream

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated March 27, 2014

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  • ACTIVE INGREDIENT

    Diphenhydramine hydrochloride, USP 2%

    Zinc acetate, USP 0.1%

  • PURPOSE

    Topical analgesic

    Skin protectant

  • USES

    For the temporary relief of pain and itching associated with

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

    For external use only

  • DO NOT USE

    • on large areas of the body
    • with any other product containing diphenhydramine, even one taken by mouth
  • ASK A DOCTOR BEFORE USE

    • on chicken pox
    • on measles
  • WHEN USING THIS PRODUCT

    • avoid contact with the eyes
  • STOP USE AND ASK A DOCTOR IF

    • condition gets worse
    • symptoms persist for more than 7 days or clear up and occur again within a few days
  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS

    • do not use more often than directed
    • 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
  • OTHER INFORMATION

    • Store between 59°-86°F (15°-30°C).
  • INACTIVE INGREDIENT

    cetyl alcohol, methylparaben, polysorbate 60, propylene glycol, purified water, sorbitan monostearate

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    NDC 0363-0525-56

    Walgreens  The Brand America Trusts®

    Compare to the active ingredients inBENADRYL® EXTRA STRENGTH ITCH STOPPING CREAM*

    Wal-dryl

    Topical Analgesic/Skin Protectant

    ITCH RELIEF

    MAXIMUM STRENGTH

    2% Diphenhydramine Hydrochloride, USP and 0.1% Zinc Acetate, USP

    Temporary Relief of Itch and Pain due to

    • Insect Bites • Minor Skin Irritations •Rashes from Poison Ivy, Poison Oak or Poison Sumac

    PHARMACIST RECOMMENDED

    NET WT. 1 OZ (28 g)

    05250111F1  VC110348

    *This product is not affiliated with, manufactured by, or produced by the makers or owners of Benadryl®.

    Made in USA

    Distributed by: Walgreen Co.,

    200 Wilmot Rd., Deerfield, IL 60015-4616

    Quality Guaranteed

    100% Satisfaction Guaranteed with all Walgreens Products or Your Money Back. www.walgreeens.com

    Wal-Dryl
  • INGREDIENTS AND APPEARANCE
    WAL-DRYL 
    diphenhydramine hydrochloride and zinc acetate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0122
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE2 mg  in 1 g
    ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION0.1 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0122-011 in 1 CARTON
    128 g in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart34803/27/2014
    Labeler - Walgreen Company (008965063)
    Registrant - NeoPharm Co., Ltd. (631101883)
    Establishment
    NameAddressID/FEIBusiness Operations
    NeoPharm Co., Ltd.631101883manufacture(0363-0122)
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