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

  • NDC Code(s): 49527-076-01
  • Packager: CLINIQUE LABORATORIES LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 19, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Aluminum chlorohydrate 18.20%

  • Purpose

    Antiperspirant

  • Use

    Reduces underarm wetness

  • Warnings

    For external use only

    Do not use on broken skin

    Stop use if 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\aqua\eau • ceteth-2 • ppg-11 stearyl ether • steareth-20 • myristalkonium chloride • quaternium-14 • sorbic acid • trisodium edta [iln37802]

  • PRINCIPAL DISPLAY PANEL - 75 ml Bottle Label

    C
    CLINIQUE

    antiperspirant-
    deodorant
    roll-on

    ALUMINUM CHLOROHYDRATE

    2.5 FL.OZ.LIQ./75 ml e

    PRINCIPAL DISPLAY PANEL - 75 ml Bottle Label
  • INGREDIENTS AND APPEARANCE
    ANTIPERSPIRANT-DEODORANT ROLL-ON 
    aluminum chlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49527-076
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE182 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETETH-2 (UNII: 7H8VAM7778)  
    POLYPROPYLENE GLYCOL 11 STEARYL ETHER (UNII: S4G2J0Y0LG)  
    STEARETH-20 (UNII: L0Q8IK9E08)  
    MYRISTALKONIUM CHLORIDE (UNII: 0W255OL75T)  
    QUATERNIUM-14 (UNII: ZGE94G6AGI)  
    SORBIC ACID (UNII: X045WJ989B)  
    EDETATE TRISODIUM (UNII: 420IP921MB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49527-076-0175 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01901/15/2020
    Labeler - CLINIQUE LABORATORIES LLC (044475127)
    Registrant - Estee Lauder Companies Inc. (790802086)
    Establishment
    NameAddressID/FEIBusiness Operations
    Whitman Laboratories Ltd.216866277manufacture(49527-076) , pack(49527-076) , label(49527-076)
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