BZK PADS (BENZALKONIUM CHLORIDE) SWAB [DYNAREX CORPORATION]

BZK PADS (BENZALKONIUM CHLORIDE) SWAB [DYNAREX CORPORATION]
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NDC 67777-244-01
Set ID 10454042-ff2e-44ce-b2e2-436cc004897f
Category HUMAN OTC DRUG LABEL
Packager Dynarex Corporation
Generic Name
Product Class
Product Number
Application Number PART333A
  • ACTIVE INGREDIENT

    Active Ingredient                                     Purpose

    Benzalkonium Chloride 0.13% v/v              Antiseptic

  • Warnings

    For external use only

  • Purpose

    Benzalkonium_OB

    First aid antiseptic to help prevent skin infection in minor cuts, scrapes and burns
    Antiseptic cleansing
    Perineal and maternity care

  • Stop use if

    Stop Use if:

    • irritation and redness develop
    • if condition persists for more than 72 hours, consult a physician.
  • Indications & Usage

    General antiseptic

    Ask a doctor before use if you have
    deep or puncture wounds
    animal bites
    serious burns

  • Dosage & Administration

    Dosage and Administration:
    Tear at notch, remove towelette, use only once
    As a first aid antiseptic

    clean affeected area
    apply 1 to 3 times daily
    may be covered with a sterile bandage
    if bandaged let dry first

  • Keep out of reach of children


    Keep out of reach of children

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

  • Do not use

    Do not use

    • as a first aid antiseptic for more than 1 week
    • in the eyes
    • over large areas of the body
  • Inactive ingredient section

    Inactive ingredient(s): chlorothymal, ispropyl alcohol, water

  • Principal Display Panel

    Benzalkonium_OB.jpg

    Benzalkonium_OB

  • INGREDIENTS AND APPEARANCE
    BZK PADS 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-244
    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
    CHLOROTHYMOL (UNII: LJ25TI0CVT)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-244-0110 in 1 CASE04/05/2011
    1100 in 1 BOX
    10.55 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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