Label: BZK- benzalkonium chloride swab

  • NDC Code(s): 50685-010-25
  • Packager: Dalian Goodwood Medical Care Ltd.
  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated May 25, 2023

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  • Drug Facts

  • Active Ingredients

    Benzalkonium chloride, 0.1 %

    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 or apply over large areas of the body.
    • In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor.

    Stop use and consult a doctor

    if the condition persists or gets worse.

    Do not use

    for longer than 1 week unless directed by a doctor.

    Keep out of reach of children

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

  • Directions

    • Tear open pouch and use as part of your daily cleansing routine.
    • Chean the affected area.
    • Apply this product on the area 1 to 3 times daily.
    • May be covered with a sterile bandage.
    • If bandaged, let dry first.
  • Other information

    Store at room temperature between 59-86 F (15-30 C)

  • Inactive ingredients

    Purified water

  • Questions or comments?

    Call 866-322-4634,

    weekdays between 8:00 am and 6:00 pm EST

  • Product Label

    BZK

  • INGREDIENTS AND APPEARANCE
    BZK 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50685-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50685-010-253 in 1 BOX03/19/201504/30/2026
    11 g in 1 APPLICATOR; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/19/201504/30/2026
    Labeler - Dalian Goodwood Medical Care Ltd. (529575699)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dalian Goodwood Medical Care Ltd.529575699manufacture(50685-010)
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