BZK TOWELETTE- benzalkonium chloride swab

BZK Towelette by

Drug Labeling and Warnings

BZK Towelette by is a Otc medication manufactured, distributed, or labeled by Dukal Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

Benzalkonium Chloride, 0.133% w/v

Purpose

First Aid Antiseptic

Use

Antiseptic Cleansing of face, hands and body without soap and water. Air dries in seconds.

Do Not Use

In the eyes or apply over large areas of the body.

Stop Use

If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

Caution

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Tear open packet, unfold and use as a washcloth.

Inactive Ingredients

Sodium Bicarbonate, Water

Principal Display Panel - 1.4 mL Pouch Label

Dukal

CORPORATION

REF 855

NDC: 65517-0004-1

BZK ANTISEPTIC

TOWELETTE

Contains Benzalkonium Chloride

1/Pouch LAte

Manufactured For: DUKAL CORPORATION

Ronkonkoma, NY 11779 www.dukal.com

Questions? 1-800-243-0741

Made in China D07110604 Rev7

Principal Display Panel - 2.1 mL Pouch Label

Dukal™

CORPORATION

REF 855C

NDC: 65517-0004-2

NON-Sterile

BZK TOWELETTE

Contains Benzalkonium Chloride

For External Use Only

1/Pouch

DUKAL CORPORATION

(631) 656-3800

Ronkonkoma, NY 11779

www.dukal.com

Made in China

INGREDIENTS AND APPEARANCE

BZK TOWELETTE  
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65517-0004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.33 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: 65517-0004-1	1.4 mL in 1 POUCH; Type 0: Not a Combination Product	01/01/2006
2	NDC: 65517-0004-2	2.1 mL in 1 POUCH; Type 0: Not a Combination Product	01/01/2006

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2006

Labeler - Dukal Corp (791014871)