Label: PURAX- aluminum chloride hexahydrate liquid

  • NDC Code(s): 76118-0003-1
  • Packager: Purax International GmbH
  • Category: HUMAN OTC DRUG LABEL

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 November 26, 2018

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  • Active ingredient

    ALUMINUM CHLORIDE HEXAHYDRATE 15%

  • Purpose

    Antiperspirant

  • Uses

    Reduces underarm perspiration

  • Warnings

    For external use only

  • Do not use

    on broken skin or face

  • 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 once a week to clean underarms before going to bed. Apply to underarms only.

  • Inactive ingredients

    Water (Aqua), Caprylic/Capric Triglyceride, Aloe Barbadensis Gel, Glycerin, Cetyl Palmitate, Ceteareth-20, Phenoxyethanol, Cetyl Alcohol, Glyceryl Stearate, Cetearyl Alcohol, Ceteareth-12, Fregrance, Tocopheryl Acetate, Ethylhexylglycerin Citric Acid, Sodium Benzoate, Potassium Sorbate, BHT

  • Questions?

    Sweat Solutions LLC

    1309 S. Flower St.

    Burbank, CA 92502

  • Principal Display Panel

    Purax

    Pure Pads

    Unisex

    Antiperspirant Deodorant

    Roll On

    Clinical Strength

    Manufactured for PURAX by

    Schrofner Cosmetics

    Robinigstrate Be 26a

    5020 Salzburg, Austria

    LOT/EXP: See Bottom

    Made in Austria, EU

    Label

  • INGREDIENTS AND APPEARANCE
    PURAX 
    aluminum chloride hexahydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76118-0003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE15 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    ALOE (UNII: V5VD430YW9)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETYL PALMITATE (UNII: 5ZA2S6B08X)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETEARETH-12 (UNII: 7V4MR24V5P)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76118-0003-150 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product02/17/201412/31/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35002/17/201412/31/2023
    Labeler - Purax International GmbH (300029336)
    Establishment
    NameAddressID/FEIBusiness Operations
    Schrofner Cosmetics Gmbh300226873manufacture(76118-0003)
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