BZK PADS - benzalkonium chloride swab 
Dynarex Corporation

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.

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Active Ingredient                                     Purpose

Benzalkonium Chloride 0.13% v/v              Antiseptic

Use benzalkonium chloride towelette

            Benzalkonium_Towelette

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

Warnings

For external use only

Indications and Usage


General antiseptic

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

Stop use if

Stop Use if:

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

Directions

Directions:

  • 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(s)

Benzalkonium_Towelette.jpg

Benzalkonium_Towelette

BZK PADS 
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
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
Packaging
#Item CodePackage Description
1NDC:67777-245-0110 in 1 CASE
1100 in 1 BOX
1.55 mL in 1 PACKET
2NDC:67777-245-021000 in 1 CASE
2.55 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)

Revised: 03/2013
Document Id: a2dd2805-32c9-40c0-bd86-09aa93ec37c9
Set id: 1409c437-ff17-481d-94be-87dd6d463ba9
Version: 16
Effective Time: 20130305
 
Dynarex Corporation