DAWNMIST ALCOHOL HAND SANITIZER (ALCOHOL) GEL [DUKAL CORPORATION]

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DAWNMIST ALCOHOL HAND SANITIZER (ALCOHOL) GEL [DUKAL CORPORATION]
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NDC 65517-1007-1, 65517-1007-2, 65517-1007-3, 65517-1007-4, 65517-1007-5
Set ID caa4c61d-efc6-41c6-bbef-de414d62ab10
Category HUMAN OTC DRUG LABEL
Packager Dukal Corporation
Generic Name
Product Class
Product Number
Application Number PART333E
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  • Active Ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antibacterial Agent

  • Use:

    For hand washing to decrease bacteria on skin.

  • Warnings

    Flammable.
    Keep away from heat or flame.
    For external use only.

    Do not use in the eyes ■ In rare instances of irritation,
    discontinue use if irritation and redness develop ■ If
    condition persists for more than 72 hours, consult a
    physician

  • Keep out of reach of children.

    ■ If swallowed, contact a physician or poison center ■ Use only as directed

  • Directions:

    To decrease bacteria on skin, apply a small amount to palm. Briskly rub covering hands with product until dry.

  • Inactive Ingredients:

    Water, Glycerin, Propylene Glycol, DMDM Hydantoin, Aminomethyl Propanediol, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Vera Leaf Extract, Tocopherol

  • Package Label

    Hand SanitizerNDC 65517-1007-3

    DawnMist

    Handwashing

    Hand Sanitizer

    Citrus Scent

    Kills 99.99% of Germs

    4 FL. OZ. (118ml)

  • INGREDIENTS AND APPEARANCE
    DAWNMIST ALCOHOL HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65517-1007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL700 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65517-1007-11.5 mL in 1 PACKET; Type 0: Not a Combination Product01/14/2013
    2NDC:65517-1007-259 mL in 1 BOTTLE; Type 0: Not a Combination Product01/14/2013
    3NDC:65517-1007-3118 mL in 1 BOTTLE; Type 0: Not a Combination Product01/14/2013
    4NDC:65517-1007-4236 mL in 1 BOTTLE; Type 0: Not a Combination Product01/14/2013
    5NDC:65517-1007-5236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/14/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/14/2013
    Labeler - Dukal Corporation (791014871)
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