BZK TOWELETTE- benzalkonium chloride swab

BZK Towelette by

Drug Labeling and Warnings

BZK Towelette by is a Otc medication manufactured, distributed, or labeled by Acme United Corporation. 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

Carton Image

INGREDIENTS AND APPEARANCE

BZK TOWELETTE 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-7112(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: 0924-7112-00	1.4 mL in 1 POUCH; Type 0: Not a Combination Product	04/16/2019
2	NDC: 0924-7112-01	10 in 1 CARTON	04/16/2019
2		1.4 mL in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 0924-7112-02	10 in 1 CARTON	04/16/2019
3		1.4 mL in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 0924-7112-03	25 in 1 CARTON	04/16/2019
4		1.4 mL in 1 POUCH; Type 0: Not a Combination Product
5	NDC: 0924-7112-04	50 in 1 CARTON	04/16/2019
5		1.4 mL in 1 POUCH; Type 0: Not a Combination Product
6	NDC: 0924-7112-05	100 in 1 CARTON	04/16/2019
6		1.4 mL in 1 POUCH; 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	04/16/2019

Labeler - Acme United Corporation (001180207)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		045924339	relabel(0924-7112) , repack(0924-7112)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		080119599	relabel(0924-7112) , repack(0924-7112)