KIEHLS SINCE 1851 BODY FUEL ANTIPERSPIRANT AND DEODORANT (ALUMINUM CHLOROHYDRATE) LOTION [L'OREAL USA PRODUCTS INC]

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  • KIEHLS SINCE 1851 BODY FUEL ANTIPERSPIRANT AND DEODORANT (ALUMINUM CHLOROHYDRATE) LOTION [L'OREAL USA PRODUCTS INC]

KIEHLS SINCE 1851 BODY FUEL ANTIPERSPIRANT AND DEODORANT (ALUMINUM CHLOROHYDRATE) LOTION [L'OREAL USA PRODUCTS INC]
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NDC 49967-639-01
Set ID f5ef03e1-aa3b-4cc5-8734-7b912daf0c79
Category HUMAN OTC DRUG LABEL
Packager L'Oreal USA Products Inc
Generic Name
Product Class
Product Number
Application Number PART350
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  • Active ingredient

    Aluminum chlorohydrate 12%

  • Purpose

    Antiperspirant

  • Use

    reduces underarm wetness

  • Warnings

    For external use only

  • Do not use

    on broken skin

  • Stop use if

    rash or irritation occurs

  • Ask a doctor before use if

    you have kidney disease

  • Keep out of reach of children.

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

  • Directions

    apply to underarms only

  • Inactive ingredients

    water, cetearyl alcohol, fragrance, ceteareth-33, perlite, dimethicone, phenoxyethanol, pentylene glycol, limonene, caffeine, tocopheryl acetate, zinc gluconate, ascorbyl glucoside, linalool, citral

  • PRINCIPAL DISPLAY PANEL

    image of a carton

  • PRINCIPAL DISPLAY PANEL

    image of a bottle

  • INGREDIENTS AND APPEARANCE
    KIEHLS SINCE 1851 BODY FUEL ANTIPERSPIRANT AND DEODORANT 
    aluminum chlorohydrate lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-639
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE120 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETEARETH-33 (UNII: R42C2O714B)  
    PERLITE (UNII: 0SG101ZGK9)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    CAFFEINE (UNII: 3G6A5W338E)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ZINC GLUCONATE (UNII: U6WSN5SQ1Z)  
    ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    CITRAL (UNII: T7EU0O9VPP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-639-011 in 1 CARTON03/28/2018
    175 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35003/28/2018
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    Fareva Richmond, Inc.969523245manufacture(49967-639)
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