Label: ANTI ITCH- diphenhydramine hydrochloride, zinc acetate cream

  • NDC Code(s): 41250-622-16, 41250-622-64
  • Packager: Meijer Distribution Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 November 29, 2018

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  • Active ingredients

    Diphenhydramine hydrochloride 2%

    Zinc acetate 0.1%

  • Purpose

    Topical analgesic

    Skin protectant

  • Uses

    •
    temporarily relieves pain and itching associated with:
    •
    insect bites
    •
    minor burns
    •
    sunburn
    •
    minor skin irritations
    •
    minor cuts
    •
    scrapes
    •
    rashes due to poison ivy, poison oak and poison sumac
    •
    dries the oozing and weeping of poison ivy, poison oak and poison 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 worsens or does not improve within 7 days
    •
    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 than directed
    •
    adults and children 2 years of age and older: apply to affected area no more than 3 to 4 times daily
    •
    children under 2 years of age: ask a doctor
  • Other information

    •
    store at 20°-25°C (68°-77°F)
  • Inactive ingredients

    cetyl alcohol, diazolidinyl urea, methylparaben, PEG-2 stearate, PEG-20 stearate, propylene glycol, propylparaben, purified water

  • Questions or comments?

    1-800-719-9260

  • Principal Display Panel

    EXTRA STRENGTH

    anti-itch cream

    Topical Analgesic | Skin Protectant

    Relieves Pain and Itching Due to Minor Skin Irritations

    Fast Relief for Most Outdoor Itches

    Compare to Extra Strength Benadryl® Cream active ingredients

    EXTRA STRENGTH

    anti-itch cream

    Topical Analgesic | Skin Protectant

    Relieves Pain and Itching Due to Minor Skin Irritations

    INSECT BITES | POISON IVY, OAK, SUMAC | SUNBURN

    MOSQUITO BITES | MINOR CUTS & SCRAPES

    NET WT 1 OZ (28 g)

    anti-itch cream image
  • INGREDIENTS AND APPEARANCE
    ANTI ITCH 
    diphenhydramine hydrochloride, zinc acetate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-622
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE2 g  in 100 g
    ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    PEG-2 STEARATE (UNII: 94YQ11Y95F)  
    PEG-20 STEARATE (UNII: NBX892EA57)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41250-622-162 in 1 CARTON04/20/201006/01/2018
    128 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:41250-622-641 in 1 CARTON03/17/2010
    228 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34803/17/2010
    Labeler - Meijer Distribution Inc (006959555)
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