Label: HEALMUSZ ECZEMA- hydrocortisone 1% cream

  • NDC Code(s): 84010-008-01
  • Packager: Jiangxi Hemei Pharmaceutical Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 17, 2024

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  • Active Ingredient

    Hydrocortisone 1%

  • Purpose

    Anti-itch

  • Use

    temporarily relieves the itching and discomfort associated with minor skin irritations, rashes, and inflammation, and due
    to eczema other uses of this product should only be under the advice and supervision of a doctor

  • Warnings

    For external use only

  • Do not use

    or the treatment of diaper rash. Consult a doctor.

  • When Using

    avoid contact with eyes do not use more than directed unless told to do so by a doctor.

  • Stop Use

    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

  • Ask Doctor

    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

  • Keep Oot Of Reach Of Children

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

  • Directions

    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: ask a doctor

  • Other information

    contents filled by weight, not volume

  • Inactive ingredients

    Borneol, Cetyl Alcohol, Glycerin, Glyceryl 1-Stearate, Menthol, Nifedipine, etc.

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    HEALMUSZ ECZEMA 
    hydrocortisone 1% cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84010-008
    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
    GLYCERIN (UNII: PDC6A3C0OX)  
    NIFEDIPINE (UNII: I9ZF7L6G2L)  
    BORNEOL (UNII: M89NIB437X)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    GLYCERYL 1-STEARATE (UNII: 258491E1RZ)  
    MENTHOL (UNII: L7T10EIP3A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84010-008-01100 g in 1 BOTTLE; Type 0: Not a Combination Product02/17/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00502/17/2024
    Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jiangxi Hemei Pharmaceutical Co., Ltd724892056label(84010-008) , manufacture(84010-008)
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