DAWNMIST ANTIPERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) LIQUID [DUKAL CORPORATION]

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DAWNMIST ANTIPERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) LIQUID [DUKAL CORPORATION]
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NDC 65517-1009-1
Set ID 86388cda-695a-4793-afa1-8d1abcc6ec06
Category HUMAN OTC DRUG LABEL
Packager Dukal Corporation
Generic Name
Product Class
Product Number
Application Number PART350
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  • Active Ingredient

    Aluminum Chlorohydrate 4.5%

  • Purpose

    Antiperspirant

    Use

    • Reduces underarm perspiration.
  • Warnings

    For external use only.

  • Do not use

    on broken skin.

  • Discontinue use if

    ■irritation and redness
    develop ■ If condition persists for more than 72
    hours consult a doctor.

  • Ask a doctor before use

    if you have kidney disease.

  • Keep out of reach of children

    ■If swallowed, get medical help and contact Poison Control Center right away ■ Use only as directed

  • Directions

    Apply to underarms only.

  • Inactive Ingredients

    Water, Mineral Oil, Cetyl Alcohol, Ceteareth-20, Isopropyl Palmitate, Magnesium Aluminum Silicate, Methylparaben, Fragrance, Sodium Benzoate, Propylparaben

  • Package Label

    DawnMist

    DEODERANTS

    Roll-On

    Antiperspirant

    REDUCES WETNESS & ODOR

    FRESH SCENTt

    1.5 FL. OZ. (44ml) label1

  • INGREDIENTS AND APPEARANCE
    DAWNMIST ANTIPERSPIRANT DEODORANT 
    aluminum chlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65517-1009
    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)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65517-1009-144 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product01/10/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35001/10/2013
    Labeler - Dukal Corporation (791014871)
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