Label: ITCH RELIEF- diphenhydramine hcl, zinc acetate spray

  • NDC Code(s): 41250-295-20
  • Packager: Meijer Distribution, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 11, 2024

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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 or 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 KENVUE, INC., DISTRIBUTOR OF BENADRYL ® EXTRA STRENGTH SPRAY.

  • Adverse Reactions

    DIST. BY MEIJER DISTRIBUTION, INC.

    GRAND RAPIDS, MI 49544

    www.meijer.com

    PID 4430883

  • principal display panel

    NDC 41250-295-20

    TEAR HERE

    COMPARE TO BENADRYL ® SPRAY ACTIVE INGREDIENTS*

    meijer

    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 DrugM01711/01/2018
    Labeler - Meijer Distribution, Inc (006959555)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(41250-295)
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