Label: HYDROCORTISONE cream

  • NDC Code(s): 0363-1973-16, 0363-1973-26, 0363-1973-64
  • Packager: Walgreen Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 15, 2024

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  • Active ingredient

    Hydrocortisone 1%

  • Purpose

    Anti-itch

  • Uses

    •
    temporarily relieves itching associated with minor skin irritations, inflammation, and rashes due to:
    •
    eczema
    •
    psoriasis
    •
    poison ivy, oak, sumac
    •
    insect bites
    •
    detergents
    •
    jewelry
    •
    cosmetics
    •
    soaps
    •
    seborrheic dermatitis
    •
    temporarily relieves external anal and genital itching
    •
    other uses of this product should be only under the advice and supervision of a doctor
  • Warnings

    For external use only

    Do not use

    •
    in the genital area if you have a vaginal discharge. Ask a doctor.
    •
    for the treatment of diaper rash. Ask a doctor.

    When using this product

    •
    avoid contact with the eyes
    •
    do not use more than directed unless told to do so by a doctor
    •
    do not put directly into the rectum by using fingers or any mechanical device or applicator

    Stop use and ask a doctor if

    •
    condition worsens
    •
    rectal bleeding occurs
    •
    symptoms persist for more than 7 days or clear up and occur again within a few days, and do not begin use of any other hydrocortisone product unless you have asked a doctor

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

  • Directions

    •
    for itching of skin irritation, inflammation, and rashes:
    •
    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: do not use, ask a doctor
    •
    for external anal and genital itching, adults:
    •
    when practical, clean the affected area with mild soap and warm water and rinse thoroughly
    •
    gently dry by patting or blotting with toilet tissue or a soft cloth before applying
    •
    apply to affected area not more than 3 to 4 times daily
    •
    children under 12 years of age: ask a doctor
  • Other information

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

    aloe barbadensis leaf juice, aluminum sulfate, calcium acetate, cetearyl alcohol, cetyl alcohol, cholecalciferol, dextrin, glycerin, isopropyl palmitate, light mineral oil, maltodextrin, methylparaben, propylene glycol, propylparaben, purified water, retinyl palmitate, sodium cetearyl sulfate, sodium lauryl sulfate, tocopherol, white petrolatum, white wax, zea mays (corn) oil

  • Questions or comments?

    1-800-719-9260

  • Principal Display Panel

    Walgreens

    WALGREENS PHARMACIST RECOMMENDED

    Compare to the active ingredient in Cortizone●10® Plus

    Maximum Strength + Vitamins A, D & E + Aloe

    Fights itch fast with moisturizing relief for:

    ● Skin irritations, rashes, redness, inflammation, eczema & psoriasis

    ULTRA-MOISTURZING

    Hydrocortisone Cream

    10 MOISTURIZERS ENRICHED WITH VITAMINS & ALOE / HYDROCORTISONE 1% / ANTI-ITCH CREAM

    NET WT 1 OZ (28 g)

    Hydrocortizone Cream Carton Image 1
    Hydrocortizone Cream Carton Image 2
  • INGREDIENTS AND APPEARANCE
    HYDROCORTISONE 
    hydrocortisone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-1973
    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
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALUMINUM SULFATE (UNII: 34S289N54E)  
    CALCIUM ACETATE (UNII: Y882YXF34X)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    CORN OIL (UNII: 8470G57WFM)  
    ICODEXTRIN (UNII: 2NX48Z0A9G)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-1973-161 in 1 CARTON01/09/2018
    156 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:0363-1973-641 in 1 CARTON01/09/2018
    228 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:0363-1973-262 in 1 CARTON01/09/2018
    356 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/09/2018
    Labeler - Walgreen Company (008965063)
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