Label: UP AND UP ANTI ITCH- hydrocortisone cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 09/13

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

  • Active ingredient

    Hydrocortisone 1%

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  • Purpose

    Anti-itch

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  • 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
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  • 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
    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
    rectal bleeding occurs

    Keep out of reach of children.

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

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  • 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
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  • Other information

    store at 20°-25°C (68°-77°F)
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  • 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

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  • Questions?

    Call 1-800-910-6874

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  • Principal Display Panel

    Compare to active ingredient in Cortizone - 10® Plus

    anti-itch cream

    maximum strength

    hydrocortisone 1%

    NET WT 1 OZ (28 g)

    anti-itch cream

    maximum strength

    hydrocortisone 1%

    relieves itch fast

    plus 10 moisturizers

    NET WT 1 OZ (28 g)

    Target Anti-Itch Cream 1.jpg
    Target Anti-Itch Cream 2.jpg
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  • INGREDIENTS AND APPEARANCE
    UP AND UP ANTI ITCH 
    hydrocortisone cream
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:11673-973
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HYDROCORTISONE (HYDROCORTISONE) HYDROCORTISONE 1 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    ALOE VERA LEAF  
    ALUMINUM SULFATE  
    CALCIUM ACETATE  
    CETOSTEARYL ALCOHOL  
    CETYL ALCOHOL  
    CHOLECALCIFEROL  
    GLYCERIN  
    ISOPROPYL PALMITATE  
    LIGHT MINERAL OIL  
    MALTODEXTRIN  
    METHYLPARABEN  
    PROPYLENE GLYCOL  
    PROPYLPARABEN  
    WATER  
    VITAMIN A PALMITATE  
    SODIUM CETOSTEARYL SULFATE  
    SODIUM LAURYL SULFATE  
    TOCOPHEROL  
    PETROLATUM  
    WHITE WAX  
    CORN OIL  
    Product Characteristics
    Color WHITE Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11673-973-64 1 in 1 CARTON
    1 28 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part348 03/18/2013
    Labeler - Target Corporation (006961700)
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