Label: DIPHENHYDRAMINE HCL AND ZINC ACETATE- diphenhydramine hydrochloride, zinc acetate cream

  • NDC Code(s): 45802-358-03
  • Packager: Padagis Israel Pharmaceuticals Ltd
  • 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 10, 2021

If you are a consumer or patient please visit this version.

  • 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 Itch Relief Cream

    Relieves Itches from Insect Bites and Skin Irritations

    Compare to Extra Strength Benadryl® Cream active ingredients

    Diphenhydramine HCl & Zinc Acetate

    Extra Strength Itch Relief Cream

    Topical Analgesic - Skin Protectant

    NET WT 1 OZ (28 g)

    Perrigo Diphenhydramine HCl & Zinc Acetate image 1
    Perrigo Diphenhydramine HCl & Zinc Acetate image 2
  • INGREDIENTS AND APPEARANCE
    DIPHENHYDRAMINE HCL AND ZINC ACETATE 
    diphenhydramine hydrochloride, zinc acetate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:45802-358
    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)  
    PEG-2 STEARATE (UNII: 94YQ11Y95F)  
    PEG-20 STEARATE (UNII: NBX892EA57)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:45802-358-031 in 1 CARTON12/05/2005
    128 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 finalpart34812/05/2005
    Labeler - Padagis Israel Pharmaceuticals Ltd (600093611)