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.

----------

Benzalkonium Chloride Pads

Active Ingredient                                     Purpose

Benzalkonium Chloride 0.13% v/v              Antiseptic

Purpose

  Purpose

  • 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

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.

Dosage and Administration

Dosage and Administration

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): water

Principal display panel(s)

Benzalkonium_Towelette.jpg

Benzalkonium_Towelette

BZK PADS 
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUG LABELItem 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 DescriptionMarketing Start DateMarketing End Date
1NDC:67777-245-01100 in 1 BOX
10.55 mL in 1 PACKET
2NDC:67777-245-021000 in 1 BOX
20.55 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: 5/2013
Document Id: e54637e7-8a30-41cb-ad65-7d17b92f7da3
Set id: 1409c437-ff17-481d-94be-87dd6d463ba9
Version: 21
Effective Time: 20130510
 
Dynarex Corporation