Label: BENZALKONIUM CHLORIDE- handy solutions first aid kit kit

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

Drug Label Information

Updated March 6, 2024

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  • Active ingredient

    Benzalkonium Chloride, 0.13%

  • Purpose

    Antiseptic

  • Use

    First Aid to help reduce the risk of infection in minor cuts, scrapes and burns.

  • Warnings

    For external use only.

    Do not use in the eyes or over large areas of the body

    Ask a doctor before use if you have deep or puncture wounds or serious burns.

    Stop use and ask a doctor if condition persists or gets worse

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control center right away

  • Directions

    Antiseptic Wipes:

    Clean the affected area.

    Bandages:

    Anti-bacterial bandages are to be applied topically to the skin for the management of minor cuts, minor scrapes

  • Inactive ingredients

    Sodium Bicarbonate, Purified Water

  • Principal Display Panel

    Handy Solutions First Aid Kit

    BZK Wipe

  • INGREDIENTS AND APPEARANCE
    BENZALKONIUM CHLORIDE 
    handy solutions first aid kit kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67751-228
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67751-228-011 in 1 KIT; Type 0: Not a Combination Product05/01/2024
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 15 POUCH 8 mL
    Part 1 of 1
    BENZALKONIUM CHLORIDE 
    mk bzk antiseptic towelette non-sterile liquid
    Product Information
    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 BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    11 in 1 PACKAGE
    11.6 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/23/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00305/01/2024
    Labeler - Navajo Manufacturing Company Inc. (091917799)
    Registrant - Navajo Manufacturing Company Inc. (136941411)
    Establishment
    NameAddressID/FEIBusiness Operations
    Changzhou Maokang Medical Products Co., Ltd421317073manufacture(67751-228)
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