Label: FUZION AB FOAM- benzalkonium chloride liquid

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

Drug Label Information

Updated November 18, 2024

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  • 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)
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