Label: ANTIBACTERIAL HAND SANITIZER- alcohol spray

  • NDC Code(s): 71160-189-05, 71160-189-10, 71160-189-20, 71160-189-25
  • Packager: TEKWELD SOLUTIONS, INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 5, 2024

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

  • Drug Facts

  • Active Ingredients

    Ethyl Alcohol 62%

    Purpose

    Antibacterial

  • Uses:

    For hand washing to decrease bacteria on the skin.

  • Warnings:

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

    When using this product

    Keep out of eyes. In case of contact with eyes, rinse with water.

    Stop use and ask a doctor

    if irritation and redness develops and persists.

    Keep out of reach of children.

    If swallowed, get medical help promptly and contact Poison Control Center.

  • Directions:

    Wet hands thoroughly with product and allow to dry without wiping.

  • Other Information:

    Store under 105°F.

  • Inactive Ingredients:

    Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water.

  • Questions or Comments?

    www.tekweld.com

  • Package Labeling:71160-189-05

    Label0

  • Package Labeling:71160-189-10

    Label02

  • Package Labeling: 70412-189-20

    Label 20

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL HAND SANITIZER 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71160-189
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL620 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71160-189-1010 mL in 1 BOTTLE; Type 0: Not a Combination Product01/09/2017
    2NDC:71160-189-055 mL in 1 BOTTLE; Type 0: Not a Combination Product01/09/2017
    3NDC:71160-189-2525 mL in 1 BOTTLE; Type 0: Not a Combination Product01/09/2017
    4NDC:71160-189-2020 mL in 1 BOTTLE; Type 0: Not a Combination Product01/09/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/09/2017
    Labeler - TEKWELD SOLUTIONS, INC. (169803389)