Your browser does not support JavaScript! BZK PADS (BENZALKONIUM CHLORIDE) SWAB [DYNAREX CORPORATION]
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RxNorm Names

BZK PADS (benzalkonium chloride) swab
[Dynarex Corporation]


Category DEA Schedule Marketing Status
HUMAN OTC DRUG LABEL OTC monograph not final
NOTE: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.
Drug Label Sections

Active Ingredient                                     Purpose

Benzalkonium Chloride 0.13% v/v              Antiseptic

Warnings

For external use only

Purpose

Benzalkonium Chloride Cleansing

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

Directions:
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

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_Chloride_Cleansing.jpg

Benzalkonium_Chloride_Cleansing

BZK PADS 
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:67777-243
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 
ALCOHOL 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67777-243-01.55 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: 1/2014
 
Dynarex Corporation

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