FIRST AID ONLY BZK ANTISEPTIC TOWELETTES- benzalkonium chloride liquid
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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First Aid Only BZK Antiseptic Towelette

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

carton label

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)

#	Item Code	Package Description	Marketing Start Date
Packaging
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	08/09/2021

Labeler - Acme United Corporation (001180207)

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

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

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