WAL-DRYL (DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE) CREAM [WALGREEN COMPANY]

WAL-DRYL (DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE) CREAM [WALGREEN COMPANY]
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NDC 0363-0122-01
Set ID 9575213f-64ca-47ac-b2bd-01f973af910b
Category HUMAN OTC DRUG LABEL
Packager Walgreen Company
Generic Name
Product Class
Product Number
Application Number PART348
  • 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)