Label: DAWNMIST ALCOHOL HAND SANITIZER- alcohol gel

  • NDC Code(s): 65517-1007-1, 65517-1007-2, 65517-1007-3, 65517-1007-4, view more
    65517-1007-5
  • Packager: Dukal LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 13, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • 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 DrugM00301/14/2013
    Labeler - Dukal LLC (791014871)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!