BZK TOWELETTE- benzalkonium chloride swab
Acme United 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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Firsat Aid Only BZK Antiseptic Towelettes

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

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.33 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	04/16/2019

Labeler - Acme United Corporation (001180207)

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

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