Label: ZEP FUZION INSTANT HAND SANITIZER- alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 20, 2023

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

View All Sections
  • 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
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    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)
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, PubMed, Biochemical Data Summary

More Info on this Drug

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