Label: DR SWEAT- aluminum chloride liquid

  • NDC Code(s): 64942-1633-1
  • Packager: Conopco Inc. d/b/a/ Unilever
  • 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 December 7, 2022

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  • DR SWEAT CLINICAL STRENGTH ANTIPERSPIRANT - aluminum chloride liquid

    Dr Sweat Clinical Strength Antiperspirant

  • Drug Facts

    Active ingredient

    Aluminum Chloride (15.0%)

  • Purpose

    Antiperspirant

  • Uses

    • reduces underarm perspiration

  • Warnings

    • For externaluse only.
    • Do not use on broken skin .
    • Ask a doctor before use if you have     kidney disease.
    • Stop use if rash or irritation occurs.

  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of reach of children.

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

  • Directions

    • Apply to underarms only
    • Apply to clean dry underarms before going to bed.

  • Inactive ingredients

    Water (Aqua), Tetrahydroxypropyl Ethylenediamine, VP/Polycarbamyl Polyglycol Ester, Phenoxyethanol, Polyacrylate Crosspolymer-6

  • Questions?

    Call toll-free 866-269-6082

  • OTHER SAFETY INFORMATION

    • Highest sweat profession available without a prescription
    • Clinically tested and proven formula
    • Simply and easy to apply
    • No fragrance or alcohol
    • Reduces sweat and odor

  • Packaging

    DRSWEAT

  • INGREDIENTS AND APPEARANCE
    DR SWEAT 
    aluminum chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1633
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE15 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    EDETOL (UNII: Q4R969U9FR)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1633-10.0284 g in 1 PACKET; Type 0: Not a Combination Product03/29/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35003/29/2019
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
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