Label: HAND SANITIZER GEL- ethanol liquid

  • NDC Code(s): 66949-137-08, 66949-137-28
  • Packager: Zep Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated October 20, 2023

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  • Active ingredient

    Ethanol 70% v/v

  • Purpose

    Antiseptic

  • Uses

    ■ To help reduce bacteria that can potentially cause disease

    ■ For use when soap and water are not available

  • Warnings

    For external use only.

    Flammable. Keep away from source of heat or fire

  • Do Not Use

    ■ on children less than 2 months of age

    ■ on open skin wounds

    ■ on broken or damaged skin

  • When using this product

    When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not inhale.

  • Stop use and ask a doctor

    Stop use and ask a doctor if irritation or redness develops and lasts.

  • Keep out of reach of children and pets

    Keep out of reach of children and pets. In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

  • Directions

    ■ For occasional and personal use.

    ■ Rub thoroughly into hands for at least 30 seconds. Allow to dry.

    ■ Children under 6 years should be supervised when using this product.

  • Other information

    ■ store at a temperature below 110 °F (43 °C).

    ■ may discolor certain fabrics or surfaces.

  • Inactive ingredients

    Water, Triisopropanolamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tocopheryl Acetate.

  • Questions?

    1-800-514-6729

  • PRINCIPAL DISPLAY PANEL

    137-4508

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER GEL 
    ethanol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-137
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    TRIISOPROPANOLAMINE (UNII: W9EN9DLM98)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-137-2815140 mL in 1 CASE; Type 0: Not a Combination Product07/05/2021
    2NDC:66949-137-082840 mL in 1 CASE; Type 0: Not a Combination Product07/05/202112/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/05/2021
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.112125310manufacture(66949-137)
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