Label: INOFOAM ANTIBACTERIAL FOAMING HAND WASH- benzalkonium chloride liquid

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

Drug Label Information

Updated November 17, 2023

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  • Drug Facts

  • Active ingredient

    Benzalkonium Chloride 0.13%

    Purpose

    Antiseptic

  • Uses

    • Handwash to help reduce bacteria on the skin that potentially can cause disease. 
    • Recommended for repeated use.
  • Warings

    For external use only.

    When using this product 

    Keep out of eyes. In case of eye contact, flush eyes with water.

    Stop use and ask a doctor if

    irritation and redness develop or if condition persists for more than 72 hours.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Wet hands with water and dispense sufficient amount of product  into cupped palm of hand. • Wash both hands thoroughly for 15 seconds. •  Rinse under running water and dry thoroughly.

  • Inactive ingredients

    Water, Sodium Lauryl Ether Sulfate, Cocamide MIPA, Sodium Sulfate,Fragrance, Magnesium Nitrate, Magnesium Chloride, Alcohol Denatured, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Red#4, FD&C Yellow #5

  • Package Labeling:

    Label02

  • INGREDIENTS AND APPEARANCE
    INOFOAM ANTIBACTERIAL FOAMING HAND WASH 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73062-033
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    ALCOHOL (UNII: 3K9958V90M)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73062-033-011 in 1 CARTON11/20/2023
    11000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/20/2023
    Labeler - Avro Enterprises, LLC (804030166)
    Establishment
    NameAddressID/FEIBusiness Operations
    Fuller Industries, Inc078704329manufacture(73062-033)
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