Label: DERMFREE WHOLE BODY DEODORANT- aluminum chlorohydrate 9%whole body deodorant cream

  • NDC Code(s): 84010-015-01
  • Packager: Jiangxi Hemei Pharmaceutical Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 30, 2024

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  • Active Ingredient

    Aluminum chlorohydrate 9%

  • Purpose

    Antiperspirant

  • Use

    .Reduces underamm sweat
    .24 hour effective protection

  • Warnings

    For external use only

  • Do not use

    on broken skin

  • When Using

    Apply to underarms only

  • Stop Use

    rash or irritation occurs

  • Ask Doctor

    Ask a doctor before use ifyou have kidney disease

  • Keep Oot Of Reach Of Children

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

  • Directions

    Apply to underarms only

  • Inactive ingredients

    Cetyl alcohol,deionized water, glycerin, GLYCERYL MONOOLEATE,GLYCERYL MONOSTEARATE,GR-270773 PHOSPHOLIPID EMULSION, Silicone Oil, zinc phenolsulfonateetc

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    DERMFREE WHOLE BODY DEODORANT 
    aluminum chlorohydrate 9%whole body deodorant cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84010-015
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE9 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERYL MONOOLEATE (UNII: C4YAD5F5G6)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    WATER (UNII: 059QF0KO0R)  
    GR-270773 PHOSPHOLIPID EMULSION (UNII: D4B2F53PBH)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ZINC PHENOLSULFONATE (UNII: 4O71YT5YB5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84010-015-0185 g in 1 BOTTLE; Type 0: Not a Combination Product04/30/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01904/30/2024
    Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jiangxi Hemei Pharmaceutical Co., Ltd724892056manufacture(84010-015)
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