Label: ZEP ALCOHOL SANITIZER- ethanol liquid

  • NDC Code(s): 66949-133-01, 66949-133-24, 66949-133-85
  • Packager: Zep Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 18, 2024

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  • Active ingredient

    Ethanol 70% v/v

  • Purpose

    Antiseptic

  • Uses

    • Hand sanitizing to decrease bacteria on skin.
    • No rinsing required.
  • Warnings

    For external use only.
    Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water.
    Flammable. Keep away from fire, flame or spark.

  • When using this product

    • Do not swallow.
    • If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.
  • Stop use and ask a doctor

    Stop use and ask a doctor if skin irritation or redness persists for more than 72 hours.

  • Keep out of reach of children and pets

    Keep out of reach of children and pets. Children must be supervised in use of this product.

  • Directions

    • Wet hands thoroughly with spray mist.
    • Rub hands together allowing liquid to contact all areas, especially around the nails and cuticles.
    • Continue rubbing vigorously until hands are dry.
    • No rinsing or toweling is required.
  • Other information

    Store at 4 to 27°C (40 to 80°F).

    Dispose in accordance with all applicable federal, state and local regulations.

  • Inactive ingredients

    Deionized water; Glycerine

  • Questions or comments?

    Call 1-877-I-BUY-ZEP (1-877-428-9937)

  • PRINCIPAL DISPLAY PANEL

    133_0900

  • INGREDIENTS AND APPEARANCE
    ZEP ALCOHOL SANITIZER 
    ethanol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-133
    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
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-133-2415140 mL in 1 CASE; Type 0: Not a Combination Product08/07/2000
    2NDC:66949-133-85208198 mL in 1 DRUM; Type 0: Not a Combination Product08/07/2000
    3NDC:66949-133-0111400 mL in 1 CASE; Type 0: Not a Combination Product08/07/2000
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/07/2000
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.112125310manufacture(66949-133)
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