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

Drug Label Information

Updated November 21, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • 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)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!