Label: ITCH RELIEF- diphenhydramine hcl, zinc acetate spray

  • NDC Code(s): 41250-295-20
  • Packager: Meijer Distribution, Inc
  • 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 April 14, 2022

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  • Active ingredients

    Diphenhydramine HCL 2%

    Zinc acetate 0.1%

  • Purpose

    External analgesic

    Skin protectant

  • Uses

    • for the temporary relief of pain and itching associated with minor skin irritations
    • dries the oozing and weeping of poison: ivy, oak, sumac
  • Warnings

    For external use only

    Flammable.  Keep away from fire or flame.

  • 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

    do not get in eyes

  • Stop use and ask a doctor if

    condition worsens or symptoms last 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 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 at 20⁰ to 25⁰ C (68⁰ to 77⁰ F)

  • Inactive ingredients

    alcohol, glycerin, povidone, purified water, tris (hydroxymethyl)aminomethane

  • Disclaimer

    *This product is not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of Benadryl Spray.

    Distributed by Meijer Distribution, Inc.

    Grand Rapids, MI 49544

    www.meijer.com

  • principal display panel

    TEAR HERE

    Meijer

    Compare to the active ingredients in Benadryl Spray*

    Itch Relief Spray

    topical analgesic

    skin protectant

    Pain & Itch Reliever

    2 FL OZ (59 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    ITCH RELIEF 
    diphenhydramine hcl, zinc acetate spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-295
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE18 mg  in 1 mL
    ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE882 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POVIDONE (UNII: FZ989GH94E)  
    WATER (UNII: 059QF0KO0R)  
    TROMETHAMINE (UNII: 023C2WHX2V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41250-295-2059 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34811/01/2018
    Labeler - Meijer Distribution, Inc (006959555)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(41250-295)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(41250-295)
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