Label: GOOD SENSE ANTI ITCH- hydrocortisone cream

  • NDC Code(s): 0113-0973-16, 0113-0973-64
  • Packager: L. Perrigo Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 18, 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.

  • 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

    Relieves Itch Fast

    Dry, Itchy Skin

    Eczema & Psoriasis

    Inflammation & Redness

    Rashes

    Skin Irritation

    Enriched With Aloe Plus Vitamins A & E

    #1 DOCTOR RECOMMENDED anti-itch active ingredient

    Ultra-Moisturizing

    Lasts 10 Hours

    Maximum Strength

    Anti-Itch Cream

    Hydrocortisone 1% Anti-Itch Cream

    Plus 10 Moisturizers

    Compare to active ingredient of Cortizone-10® Plus

    100% SATISFACTION GUARANTEED

    NET WT 2 OZ (56g)

    anti itch cream image
  • INGREDIENTS AND APPEARANCE
    GOOD SENSE ANTI ITCH 
    hydrocortisone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0113-0973
    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:0113-0973-641 in 1 CARTON03/07/200612/31/2024
    128 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:0113-0973-161 in 1 CARTON10/16/201911/30/2022
    256 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/07/200612/31/2024
    Labeler - L. Perrigo Company (006013346)
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