Label: BZK TOWELETTE- benzalkonium chloride swab

  • NDC Code(s): 65517-0004-1, 65517-0004-2
  • Packager: Dukal LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 21, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredients

    Benzalkonium Chloride, 0.133% w/v

  • Use

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

  • Purpose

    First Aid Antiseptic

  • Do Not Use

    In the eyes or apply over large areas of the body.

  • Stop Use

    If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

  • Caution

    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.

  • Inactive Ingredients

    Sodium Bicarbonate, Water

  • Principal Display Panel - 1.4 mL Pouch Label

    Dukal
    BZK ANTISEPTIC

    TOWELETTE

    Contains Benzalkonium Chloride / For External Use Only

    Not made with natural rubber latex / Single Use

    Manufactured For: Dukal, LLC

    1(800)243-0741 / Ronkonkoma, NY 11779 / dukal.com

    Made in China

    Dukal is a trademark registered in the

    US Patent & Trademark Office

    by Dukal, LLC

    1 Per Pack / NDC 65517-0004-1 REF 855

    855

  • Principal Display Panel - 2.1 mL Pouch Label

    Dukal
    BZK ANTISEPTIC

    TOWELETTE

    Contains Benzalkonium Chloride / For External Use Only

    Not made with natural rubber latex / Single Use

    Manufactured For: Dukal, LLC

    1(800)243-0741 / Ronkonkoma, NY 11779 / dukal.com

    Made in China

    Dukal is a trademark registered in the

    US Patent & Trademark Office

    by Dukal, LLC

    1 Per Pack / NDC 65517-0004-2 / REF 855C

    855C

  • INGREDIENTS AND APPEARANCE
    BZK TOWELETTE 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65517-0004
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65517-0004-11.4 mL in 1 POUCH; Type 0: Not a Combination Product01/01/2006
    2NDC:65517-0004-22.1 mL in 1 POUCH; Type 0: Not a Combination Product01/01/2006
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/01/2006
    Labeler - Dukal LLC (791014871)
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