Label: BZK PADS- benzalkonium chloride swab

  • NDC Code(s): 67777-245-01, 67777-245-02, 67777-245-04, 67777-245-05, view more
    67777-245-06, 67777-245-07, 67777-245-08, 67777-245-11, 67777-245-14, 67777-245-15, 67777-245-16, 67777-245-17, 67777-245-18
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 25, 2024

If you are a consumer or patient please visit this version.

  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    First Aid Antiseptic

  • Use(s)

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

  • 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.

  • Directions

    • 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

    Water

  • Questions?

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

  • Label

    1303 BX MNFL0101303 Label

  • Label

    1303 BX MASTER

  • Label

    1331 MC MASTER1331

  • Label

    1332 BX MASTER1332

  • Label

    1333 BX MASTER1333

  • Label

    1331 MC MNFL010

  • Label 1303UB-10

    1303UB-10_BX_MASTER1303UB-10

  • Label 1303-40

    1303-40_BX_MASTER1303-40

  • Label 1333-50

    1333-50_BX_MASTER1333-50

  • INGREDIENTS AND APPEARANCE
    BZK PADS 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-245
    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)  
    Product Characteristics
    Color    Score    
    ShapeRECTANGLESize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-245-1110000 in 1 CASE04/05/2011
    1NDC:67777-245-01100 in 1 BOX
    10.55 mL in 1 PACKET; Type 0: Not a Combination Product
    2NDC:67777-245-021000 in 1 BOX03/30/2017
    20.55 mL in 1 PACKET; Type 0: Not a Combination Product
    3NDC:67777-245-041000 in 1 CASE04/05/2011
    3NDC:67777-245-1410 in 1 BOX
    30.55 mL in 1 PACKET; Type 0: Not a Combination Product
    4NDC:67777-245-05750 in 1 CASE04/05/2011
    4NDC:67777-245-1525 in 1 BOX
    40.55 mL in 1 PACKET; Type 0: Not a Combination Product
    5NDC:67777-245-161000 in 1 CASE04/05/2011
    5NDC:67777-245-0610 in 1 BOX
    50.55 mL in 1 PACKET; Type 0: Not a Combination Product
    6NDC:67777-245-181000 in 1 CASE04/05/2011
    6NDC:67777-245-0840 in 1 BOX
    60.55 mL in 1 PACKET; Type 0: Not a Combination Product
    7NDC:67777-245-171000 in 1 CASE04/05/2011
    7NDC:67777-245-0750 in 1 BOX
    70.55 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/05/2011
    Labeler - Dynarex Corporation (008124539)
    Registrant - Dynarex Corporation (008124539)