Label: CLINIQUE ANTIPERSPIRANT DEODORANT ROLL-ON- aluminum chlorohydrate liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by 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 April 9, 2010

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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT:ALUMINUM CHLOROHYDRATE 20.00%

  • PURPOSE


    USES: DECREASES UNDERARM PERSPIRATION
  • WARNINGS

    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.

  • INDICATIONS & USAGE

    DIRECTIONS: APPLY TO UNDERARMS ONLY.

  • INACTIVE INGREDIENT

    inactive ingredients: water[] urea [] silica [] alcohol denat. [] glycine [] aluminum chloride [] butyl stearate [] sodium lauroyl sarcosinate [] alcloxa [] benzethonium chloride [] trisodium edta [] methylparaben [] propylparaben [] butylparaben  iln27821

  • PRINCIPAL DISPLAY PANEL

    PRINCIPAL DISPLAY PANEL: 

    CLINIQUE
    anti-perspirant deodorant roll-on

    ALUMINUM CHLOROHYDRATE

    2.5FL OZ./ 70ML


    CLINIQUE LABORATORIES, DIST.
    NEW YORK, NY 10022

    6183
    CLINIQUE.COM

    FOLDING CARTON

  • INGREDIENTS AND APPEARANCE
    CLINIQUE ANTIPERSPIRANT  DEODORANT ROLL-ON
    aluminum chlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49527-571
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (aluminum cation - UNII:3XHB1D032B) ALUMINUM CHLOROHYDRATE70 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49527-571-0170 mL in 1 BOTTLE, WITH APPLICATOR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35012/01/1992
    Labeler - CLINIQUE LABORATORIES INC (173047747)
    Establishment
    NameAddressID/FEIBusiness Operations
    ESTEE LAUDER COSMETICS, LTD205952385manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    ESTEE LAUDER N.V.370151326manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Len-Ron Manufacturing Division of Aramis Inc.809771152manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Aramis Inc.042918826manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Northtec Bristol949264774manufacture, relabel, repack
    Establishment
    NameAddressID/FEIBusiness Operations
    Northtec Keystone618107429manufacture, relabel, repack
    Establishment
    NameAddressID/FEIBusiness Operations
    PADC 1110482184manufacture, relabel, repack
    Establishment
    NameAddressID/FEIBusiness Operations
    Estee Lauder Pennsylvania Distribution Center 2828534516manufacture, relabel, repack
    Establishment
    NameAddressID/FEIBusiness Operations
    Estee Lauder Cosmetics, Ltd.255175580manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Estee Lauder Cosmetics, Ltd253616536manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Estee Lauder Cosmetics Distribution Center208579636manufacture, label, relabel
    Establishment
    NameAddressID/FEIBusiness Operations
    Estee Lauder Kabushiki Kaisha712808195relabel, repack
    Establishment
    NameAddressID/FEIBusiness Operations
    Whitman Laboratories Ltd.216866277manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Aveda Corporation071352058manufacture