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BZK Pads by Dynarex Corporation

Medically reviewed on March 30, 2017

Dosage form: swab
Ingredients: BENZALKONIUM CHLORIDE 1.3mg in 1mL
Labeler: Dynarex Corporation
NDC Code: 67777-245

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.

Benzalkonium Chloride Pads

Active Ingredient

Active Ingredient                                    Purpose

Benzalkonium Chloride 0.13% v/v          Antiseptic



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


​For external use only

Stop use if:

Stop use if:

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

Indications and Usage

Indications and Usage:

General antiseptic

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

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.

Dosage and Administration

Dosage and Administration


  • Tear at notch, remove towelette, use only once.

​​ ​As a first aid antiseptic:

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

Do not use:

​Do not use

  • ​as a first aid antiseptuic for more than 1 week
  • in the eyes
  • over large areas of the body

Inactive ingredients

Inactive ingredient: water

Principal Display panel

Dynarex BZK Antiseptic Towelette

1303 BZK.jpg

benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-245
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:67777-245-01100 PACKET in 1 BOX
10.55 mL in 1 PACKET
2NDC:67777-245-021000 PACKET in 1 BOX
20.55 mL in 1 PACKET
3NDC:67777-245-032070 PACKET in 1 BOX
30.55 mL in 1 PACKET
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)

Dynarex Corporation

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.