Label: ANTIBACTERIAL HAND SANITIZER- alcohol gel

  • NDC Code(s): 73145-003-01, 73145-003-02, 73145-003-03
  • Packager: ASC Marketing LTD
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 1, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Drug Facts

  • Active ingredient

    Ethyl alcohol 70%

    Purpose

    Antiseptic

  • Uses

    • for handwashing to decrease bacteria on the skin. 
    • recommended for repeated use.
  • Warnings

    For external use only.

    When using this product

    • Do not use in eyes. • Discontinue use if irritation and redness develop.

    Flammable, keep away from fire or flame.

    Keep out of reach of children.

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

    If pregnant or breast-feeding,

    ask a health professional before use.

  • Directions

    • wet hands thoroughly with product. • briskly rub hands together until dry.

  • Inactive ingredients

    Water, Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Juice, Fragrance

  • Package Labeling:

    Bottle

  • Package Labeling:

    Bottle2

  • Package Labeling:73145-003-03

    Bottle3

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73145-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73145-003-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product11/19/2020
    2NDC:73145-003-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product11/19/2020
    3NDC:73145-003-0315 mL in 1 BOTTLE; Type 0: Not a Combination Product01/20/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/19/2020
    Labeler - ASC Marketing LTD (117025198)
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

More Info on this Drug

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