Label: BZK PADS- benzalkonium chloride swab

  • NDC Code(s): 67777-243-01, 67777-243-02, 67777-243-03
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 November 29, 2022

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  • Active Ingredient

    Benzalkonium Chloride 0.13% v/v

  • Purpose

    First Aid Antiseptic

  • Uses

    • First aid to help prevent skin infection in minor cuts, scrapes, and burns.

    • Cleans and refreshes hand, face, and body without soap and water.

  • Warnings

    For external use only

    Do not use

    • As an antiseptic for more than 1 week

    • In the eyes

    Ask a doctor before use if

    you have deep or puncture wounds, animal bites, or serious burns.

    Stop use and ask a doctor if

    • Irritation and redness develop

    • Condition persists or gets worse

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Direction

    • Clean the affected area.

    • May be covered with a sterile bandage

    • If bandaged, let dry first

  • Other Information

    • Store at room temperature 15º-30ºC (59º-86ºF).

    • Avoid excessive heat.

    • Tamper evident. Do not use if packet is torn or cut.

  • Inactive ingredients

    Isopropyl Alcohol, Water, may contain Methylchloroisothiazolinone/Methylisothiazolinone

  • Questions?

    1-888-Dynarex Monday - Friday, 9AM - 5PM EST

  • Label

    1301 BX MASTER1301 Cleansing Towelettes

  • Label

    1301 BX MNFL0101301 Cleansing Towelettes

  • INGREDIENTS AND APPEARANCE
    BZK PADS 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-243
    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
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE (UNII: 15O9QS218W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-243-031000 in 1 CASE04/05/2011
    1NDC:67777-243-02100 in 1 BOX
    1NDC:67777-243-010.55 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/05/2011
    Labeler - Dynarex Corporation (008124539)
    Registrant - Dynarex Corporation (008124539)
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