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DawMist Antiperspirant Deodorant (Dukal Corporation)

Available Formats

Dosage Form Package Information Links
LIQUID 44 mL in 1 BOTTLE, WITH APPLICATOR (65517-1003-1) Label Information

Complete DawMist Antiperspirant Deodorant Information

  • 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

    â– irritation and redness
    develop â–  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

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


  • Directions

    Apply to underarms only.


  • Inactive Ingredients

    Water, Mineral Oil, Polysorbate 60, Glycerin, PEG-100 Stearate, Sorbitan Stearate, Cetearyl Alcohol, Dimethicone, Magnesium Aluminum Silicate, Glyceryl Stearate, Hydroxyethylcellulose, Fragrance, Sodium Benzoate, Methylparaben, Disodium EDTA, Propylparaben


  • Principal Display Panel - Bottle Label

    NDC 65517-1003-1

    DawnMist®

    DEODORANTS

    Roll-On
    Antiperspirant

    REDUCES WETNESS & ODOR

    FRESH SCENT

    1.5 FL. OZ. (44ml)

    Principal Display Panel - Bottle Label

  • INGREDIENTS AND APPEARANCE
    DAWMIST ANTIPERSPIRANT DEODORANT  
    aluminum chlorohydrate lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:65517-1003
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE 45 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:65517-1003-1 44 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part350 01/10/2013
    Labeler - Dukal Corporation (791014871)
    Establishment
    Name Address ID/FEI Business Operations
    Guangzhou Haishi Biological Technology Co., Ltd. 421262738 MANUFACTURE(65517-1003)