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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Benzalkonium Chloride Pads

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:

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

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 Type HUMAN OTC DRUG Item Code (Source) NDC:67777-243
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:67777-243-01 .55 mL in 1 PACKET
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 04/05/2011
Labeler - Dynarex Corporation (008124539)
Registrant - Dynarex Corporation (008124539)

Revised: 1/2014
Document Id: b8f6de9b-7011-4467-8503-fecb9c61d7c4
Set id: 87288939-cc34-4437-94ab-dcb997d6acd5
Version: 22
Effective Time: 20140124
 
Dynarex Corporation