Label: FUZION AB FOAM- benzalkonium chloride 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

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial Hand Wash

  • Uses

    For washing to decrease bacteria on hands.

  • Warnings

    For external use only.

  • Do not use

    Do not use in the eyes; if in eyes, rinse promptly and 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 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 with water.
    • Press pump to dispense product into hands.
    • Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles.
    • Rinse hands thoroughly and dry.
    • Store at 20 to 25°C (68 to 77°F).
    • Dispose in accordance with all applicable federal, state and local regulations.
  • Inactive Ingredients

    Water, Cetrimonium Chloride, Lauryl/Myristyl Amidopropyl Amine Oxide, Glycerin, Di-PPG-2 Myreth-10 Adipate, Tetrasodium Iminodisuccinate, Methylchloroisothiazolinone, Methylisothiazolinone, Fragrance, Glutaral, Citric Acid, Red 4, Yellow 5

  • Questions or comments?

    Call 1-800-I-BUY-ZEP (1-800-428-9937)

  • PRINCIPAL DISPLAY PANEL

    111_3388

  • INGREDIENTS AND APPEARANCE
    FUZION AB FOAM 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-111
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GLUTARAL (UNII: T3C89M417N)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    DI-PPG-2 MYRETH-10 ADIPATE (UNII: 4IN301M0KJ)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    WATER (UNII: 059QF0KO0R)  
    LAUROYL/MYRISTOYL AMIDOPROPYL AMINE OXIDE (UNII: HY9O6ZW9CY)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TETRASODIUM IMINODISUCCINATE (UNII: GYS41J2635)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-111-164800 mL in 1 CASE; Type 0: Not a Combination Product03/10/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/10/2017
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.112125310manufacture(66949-111)
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!