BZK PADS- benzalkonium chloride swab

BZK Pads by

Drug Labeling and Warnings

BZK Pads by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                     Purpose

Benzalkonium Chloride 0.13% v/v              Antiseptic

Warnings

For external use only

Purpose

Benzalkonium_OB

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

Dosage and Administration:
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

Benzalkonium_OB.jpg

INGREDIENTS AND APPEARANCE

BZK PADS 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-244
Route of Administration	TOPICAL

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
CHLOROTHYMOL (UNII: LJ25TI0CVT)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-244-01	10 in 1 CASE	04/05/2011
1		100 in 1 BOX
1		0.55 mL in 1 PACKET; Type 0: Not a Combination Product

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)