Label: SUAVE- 24 hour powder invisible solid antiperspirant deodorant stick

  • NDC Code(s): 64942-2235-1
  • Packager: Conopco Inc. d/b/a Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 1, 2023

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  • ACTIVE INGREDIENT

    Active ingredient

    Aluminum Chlorohydrate (20%)

  • PURPOSE

    Purpose

    antiperspirant

  • INDICATIONS & USAGE

    Uses

    reduces underarm wetness

  • WARNINGS

    Warnings

    For external use only

  • DO NOT USE

    Do not useon broken skin

  • ASK DOCTOR

    Ask a doctor before use if you havekidney disease

  • STOP USE

    Stop useif 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.

  • DOSAGE & ADMINISTRATION

    Directions

    apply to underarms only

  • INACTIVE INGREDIENT

    Inactive Ingredients
    Cyclopentasiloxane, Isopropyl Palmitate, Stearyl Alcohol, Mineral Oil, Talc, Hydrogenated Castor Oil, Fragrance (Parfum), Steareth-100, BHT.

  • QUESTIONS

    Questions?
    Call 1-800-782-8301

  • PDP 2.6 oz

    Suave Powder 2.6 oz. PDP
  • INGREDIENTS AND APPEARANCE
    SUAVE 
    24 hour powder invisible solid antiperspirant deodorant stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-2235
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE20 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    TALC (UNII: 7SEV7J4R1U)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    STEARETH-100 (UNII: 4OH5W9UM87)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-2235-174 g in 1 CONTAINER; Type 0: Not a Combination Product04/07/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01904/07/2009
    Labeler - Conopco Inc. d/b/a Unilever (001375088)
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