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

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

Stop use if:

Stop use if:

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

Indications and Usage

Indications and Usage:

General antiseptic

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

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.

Dosage and Administration

Dosage and 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​

Do not use:

​Do not use​

• ​as a first aid antiseptuic for more than 1 week
• in the eyes
• over large areas of the body

Inactive ingredients

Inactive ingredient: water

Principal Display panel

Dynarex BZK Antiseptic Towelette

1303 BZK.jpg

INGREDIENTS AND APPEARANCE

BZK PADS 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-245
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
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-245-01	100 in 1 BOX	03/30/2017
1		0.55 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 67777-245-02	1000 in 1 BOX	03/30/2017
2		0.55 mL in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 67777-245-03	2070 in 1 BOX	03/30/2017
3		0.55 mL in 1 PACKET; Type 0: Not a Combination Product
4	NDC: 67777-245-04	1000 in 1 CASE	04/05/2011
4		10 in 1 BOX
4		0.55 mL in 1 PACKET; Type 0: Not a Combination Product
5	NDC: 67777-245-05	750 in 1 CASE	04/05/2011
5		25 in 1 BOX
5		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)