Label: EQUATE CORTISONE- hydrocortisone 1% spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 27, 2023

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  • ACTIVE INGREDIENT

    Hydrocortisone 1%

  • PURPOSE

    Anti-itch

  • INDICATIONS & USAGE

    For the temporary relief of itching associated with minor skin irritation and rashes due to

    • eczema
    • poison ivy, oak, and sumac
    • cosmetics
    • soaps and detergents
    • jewelry
    • insect bites

    Other uses of this product should be only under advice and supervision of a doctor.

  • WARNINGS

    For external use only.

    Flammable. Keep away from fire or flame.

    Do not use for the treatment of diaper rash. Consult a doctor.

    When using this product

    • avoid contact with eyes. In case of contact with eyes, flush thoroughly with water
    • avoid contact with broken skin
    • do not inhale or ingest
    • contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120F.

    Stop use and ask a doctor if

    condition worsens

    symptoms last more than 7 days or clear up and occur again within a few days.

  • KEEP OUT OF REACH OF CHILDREN

    If product is swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Adults and children 2 years or older: apply to affected area not more than 3 to 4 times daily

    Children under 2 years of age: ask a doctor

    To apply to face, spray into palm of hand and gently apply.

  • INACTIVE INGREDIENT

    Alcohol denat., dimethyl isosorbide, glycerin, water.

  • PRINCIPAL DISPLAY PANEL

    Label

  • INGREDIENTS AND APPEARANCE
    EQUATE CORTISONE 
    hydrocortisone 1% spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-213
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-213-0385 g in 1 CAN; Type 0: Not a Combination Product12/27/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01712/27/2023
    Labeler - Walmart Inc (051957769)
    Registrant - Derma Care Research Labs (116817470)
    Establishment
    NameAddressID/FEIBusiness Operations
    Derma Care Research Labs116817470manufacture(79903-213)
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