FIRST AID ONLY BZK ANTISEPTIC TOWELETTES- benzalkonium chloride liquid

First Aid Only BZK Antiseptic Towelettes by

Drug Labeling and Warnings

First Aid Only BZK Antiseptic Towelettes by is a Otc medication manufactured, distributed, or labeled by Acme United Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride 0.133%

Purpose

First Aid Antiseptic

Uses

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

Warnings

Do not use

• in the eyes
• 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.

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

Purified Water, sodium bicarbonate

Questions

1-800-835-2263

PRINCIPAL DISPLAY PANEL

carton label

INGREDIENTS AND APPEARANCE

FIRST AID ONLY BZK ANTISEPTIC TOWELETTES 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-7115(NDC:59050-331)
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)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0924-7115-00	1.6 mL in 1 POUCH; Type 0: Not a Combination Product	08/09/2021
2	NDC: 0924-7115-01	10 in 1 CARTON	08/09/2021
2		1.6 mL in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 0924-7115-02	25 in 1 CARTON	08/09/2021
3		1.6 mL in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 0924-7115-03	50 in 1 CARTON	08/09/2021
4		1.6 mL in 1 POUCH; Type 0: Not a Combination Product
5	NDC: 0924-7115-04	100 in 1 CARTON	08/09/2021
5		1.6 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 Drug	M003	08/09/2021

Labeler - Acme United Corporation (001180207)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		045924339	relabel(0924-7115) , repack(0924-7115)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		080119599	relabel(0924-7115) , repack(0924-7115)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		117825595	manufacture(0924-7115)