Label: DAWNMIST ALCOHOL HAND SANITIZER- alcohol gel

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated October 13, 2023

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  • DawnMist Alcohol Hand Sanitizer

  • Active Ingredient

    Ethyl Alcohol 62%

    Purpose

    Antiseptic

  • Use

    To decrease bacteria on the skin that could cause disease

  • Warning

    For external use only

    Flammable, keep away from fire or flame.

    When using this product

    Keep out of eyes, ears and mouth. In case of contact with eyes, flush thoroughly with water.

    Stop use and ask a doctor if

    irritation or redness develops

    Keep out of reach of children

    If swallowed, get medical help or contact Poison Control Center right away.

  • Directions

    wet hands thoroughly with products and allow to dry without wiping.

    for children under 6, use only under adult supervision

  • Other Information

    Avoid freezing and excessive heat above 104°F

  • Inactive Ingredients

    Acrylates/C10-30Alkyl Acrylate Cross Polymer, Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Triethanolamine, Water

  • Principle Display Panel

    HS8004NDC 65517-1023-1

    DawnMist ®

    Hand Sanitizer

    Drug Facts

    Active Ingredient Purpose

    Ethyl alcohol 62%.........Antiseptic

    REF HS8004

    4 FL. OZ. (118 ml)

  • INGREDIENTS AND APPEARANCE
    DAWNMIST ALCOHOL HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65517-1023
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65517-1023-1118 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/09/2020
    Labeler - Dukal LLC (791014871)
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