Label: CAREALL ANTI-ITCH- diphenhydramine hydrochloride and zinc acetate cream cream

  • NDC Code(s): 51824-088-01
  • Packager: New World Imports, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 14, 2024

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  • Active Ingredients

    Diphenhydramine Hydrochloride 2%

    Zinc Acetate 0.1%

  • Purpose

    Diphenhydramine Hydrochloride 2%....Topical Analgesic

    Zinc Acetate 0.1%.............................Skin Protectant

  • Keep out of Reach of Children

    Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

  • Uses

    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 / poison sumac.
    • dries the oozing and weeping of poison ivy, poison oak and poison sumac.
  • Warnings

    For external use only.

    Due 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 eyes

    Stop use and ask a doctor if:

    • condition worsens or does not improve within 7 days
    • symptoms persists for more than 7 days or clear up and occur again within a few days

  • 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
  • Inactive Ingredients

    carbomer homopolymer type c, cetyl alcohol, glycerin, glyceryl monostearate, light mineral oil, methylparaben, polysorbate 60, propylparaben,  purified water, stearic acid

  • PRINCIPAL DISPLAY PANEL

    Anti-itch Carton

  • INGREDIENTS AND APPEARANCE
    CAREALL ANTI-ITCH 
    diphenhydramine hydrochloride and zinc acetate cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51824-088
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 g
    ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE1 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51824-088-0135 g in 1 TUBE; Type 0: Not a Combination Product07/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01707/01/2022
    Labeler - New World Imports, Inc (075372276)