Label: ZEP FUZION INSTANT HAND SANITIZER- alcohol liquid

  • 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

    ■ To help reduce germs and bacteria on the skin.
    ■ Recommended for repeated use.
    ■ No rinsing required.

  • Warnings

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

  • Do not use

    in the eye; if in eyes, rinse thoroughly with water.

  • 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 doctor

    Stop use and ask 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

    • Apply gel to hands.
    • Rub into hands for at least 20 seconds or until dry.
  • Other information

    ■ Keep container closed and stored in a dry area at temperatures between 68°F and 77°F (20°C and 25°C).
    ■ Do not reuse empty container.
    ■ Dispose in accordance with all applicable federal, state and local regulations

  • Inactive ingredients

    Deionized Water, PEG-6 (and) Acrylates/Vinyl Crosspolymer, Fragrance.

  • Questions or comments?

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

  • Package Label - Principal Display Panel

    119_3558

  • INGREDIENTS AND APPEARANCE
    ZEP FUZION INSTANT HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-119
    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/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-119-164800 mL in 1 CASE; Type 0: Not a Combination Product11/02/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/02/2020
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.112125310manufacture(66949-119)
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