FUZION AB FOAM (BENZALKONIUM CHLORIDE) LIQUID [ZEP INC.]

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FUZION AB FOAM (BENZALKONIUM CHLORIDE) LIQUID [ZEP INC.]
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NDC 66949-388-16
Set ID 5a910011-a7a4-d548-e053-2991aa0a93d9
Category HUMAN OTC DRUG LABEL
Packager Zep Inc.
Generic Name
Product Class
Product Number
Application Number PART333A
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  • Active ingredient

  • 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

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

  • KEEP OUT OF REACH OF CHILDREN

    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 INGREDIENT

    Water; Cetrimonium Chloride, Lauryl/ Myristyl Amidopropyl Amine Oxide, Glycerin, Di-PPG-2 Myreth-10 Adipate, tetrasodium iminodisuccinate, Methylchloroisothiazolinone (and) Methylisothiazolinone, fragrance, Glutaral, citric acid; Red 4; Yellow 5

  • Questions or comments?

    Call 1-877-I-BUY-ZEP

  • PRINCIPAL DISPLAY PANEL

    3388

  • INGREDIENTS AND APPEARANCE
    FUZION AB FOAM 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-388
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.013 g  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    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/METHYLISOTHIAZOLINONE MIXTURE (UNII: 15O9QS218W)  
    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:66949-388-161200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/10/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/10/2017
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.112125310manufacture(66949-388)
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