Label: DAWNMIST ANTIPERSPIRANT DEODORANT- aluminum chlorohydrate gel

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated October 13, 2023

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  • Active Ingredient

    Aluminum Chlorohydrate 4.5%

  • Purpose

    Antiperspirant

    Use

    Reduce wetness &oOdor

  • Warnings

    Ask a doctor before use if you have a kidney disease.

    Do not apply to broken skin.

    If rash develops, discontinue use.

  • Keep out of reach of children


  • Directions

    Apply to underarms only.

  • Other Ingredients

    Water, Alcohol Denat, Propylene Glycol, Hydroxyethylcellulose, PEG-40 Hydrogenated Castor Oil, PEG-12 Dimethicone Crosspolymer, Fragrance, Diazolidinyl Urea, Iodopropynyl Butylcarbamate

  • DawnMist Antiperspirant Deodorant Gel Formula 0.10oz/3ml (65517-1014-1)

    DawnMist®

    NDC: 65517-1014-1

    DEODORANTS

    Antiperspirant Deodorant

    REDUCES WETNESS & ODOR

    FRESH SCENT

    0.10 FL. OZ. (3 ml)

    Graphic

  • INGREDIENTS AND APPEARANCE
    DAWNMIST ANTIPERSPIRANT DEODORANT 
    aluminum chlorohydrate gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65517-1014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE45 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PEG-40 CASTOR OIL (UNII: 4ERD2076EF)  
    PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65517-1014-13 mL in 1 PACKET; Type 0: Not a Combination Product09/08/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01905/02/2013
    Labeler - Dukal LLC (791014871)
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