Label: BZK ANTISEPTIC SWABSTICKS 4 TRIPLE- benzalkonium chloride liquid

  • NDC Code(s): 59050-260-03
  • Packager: Changzhou Maokang Medical Products Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 21, 2024

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  • Drug Facts

  • Active ingredient

    Benzalkonium Chloride, 0.13% w/v

    Purpose

    Antiseptic

  • Uses:

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

  • Warnings:

    • 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.

    For external use only.

    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.
    • Clean the affected area.
    • Apply this product on the area 1 to 3 times daily.
    • Maybe covered with a sterile bandage.
    • If bandaged, let dry first.
  • Other information:

    • For professional and hospital use.
    • Store at room temperature.
    • Avoid excessive heat.
    • Not made with natural rubber latex.
  • Inactive ingredients:

    Purified water, sodium bicarbonate.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    BZK ANTISEPTIC SWABSTICKS 4 TRIPLE 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59050-260
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59050-260-033 in 1 POUCH11/30/2021
    16 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00311/30/2021
    Labeler - Changzhou Maokang Medical Products Co., Ltd (421317073)
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