Label: BZK- benzalkonium chloride liquid

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

Drug Label Information

Updated April 2, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients

    Benzalkonium Chloride 0.13%

  • Purpose

    First Aid Antiseptic

  • Uses

    • 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. If this happens, rinse thoroughly with water.

    Stop use and ask a doctor if irritation or redness develop and 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

    • Tear open packet, unfold and use as a washcloth. Allow hands to dry without wiping.

    Inactive ingredients purified water, alcohol

    Made in USA

  • PRINCIPAL DISPLAY PANEL – packet label

    Henry Schein REF112-6735

    NDC 0404-6735-01

    BZK TOWELETTE

    Contains Benzalkonium Chloride

    For External Use Only • Non-Sterile

    Not Made with Natural Rubber Latex

    1 single-use, premoistened towelette

    Distributed by (in US only)

    HENRY SCHEIN, Inc. 135 Duryea Road

    Melville, NY 11747 USA

    Made in China

    Rev.2024/04

    111-6735

  • INGREDIENTS AND APPEARANCE
    BZK 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0404-6735
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.0013 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0404-6735-01100 in 1 BOX12/01/2016
    12.5 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/07/2013
    Labeler - Henry Schein Inc. (012430880)
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