Label: HYDROCORTISONE cream

  • NDC Code(s): 47682-933-73
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 17, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Hydrocortisone 1.0%

  • PURPOSE

    Purpose

    Anti-itch

  • INDICATIONS & USAGE

    Uses

    • for the temporary relief of itching associated with minor skin irritations, inflammation and rashes
    • other uses of this product should be only under the advice and supervision of a doctor
  • WARNINGS

    Warnings

    For external use only

    Do not use

    • for the teatment of diaper rash. Consult a doctor

    When using this product

    • avoid contact with the eyes
    • do not begin use of any other hydrocortisone product unless you've consulted a doctor

    Stop use and ask a doctor if

    • condition worsens
    • symptoms persist for more than 7 days
    • symptoms clear up and occurs again within a few days

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

  • DOSAGE & ADMINISTRATION

    Directions

    • adults and children 2 years of age and over: apply to affected area not more than 3 to 4 times daily
    • children under 2 years of age: do not use, consult a doctor

  • SPL UNCLASSIFIED SECTION

    Other information

    • clean the affected area
    • store at room temperature (do not freeze)
    • tamper evident, do notany opened or torn packets
    • you may report a serious adverswe reaction to this product to 800-634-7680
  • Inactive ingredients

    Emulsifying wax, ethanol, methylparaben, mineral oil, paraffin, petrolatum, propylparaben, purified water, white wax

  • Medi-First Plus Hydrocortisone

    MEDI-FIRST®
    Plus

    Hydrocortisone Cream 1%

    Temporary relief of itching associated with monor skin irritations, inflamation and rashes

    25 units / Net Wt 0.9 g ( 1/32 oz)

    Item #93373

    93373 MFP

  • INGREDIENTS AND APPEARANCE
    HYDROCORTISONE 
    hydrocortisone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-933
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-933-7325 in 1 BOX04/15/2013
    10.9 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/15/2013
    Labeler - Unifirst First Aid Corporation (832947092)
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