BZK ANTISEPTIC TOWELETTE- benzalkonium chloride cloth cloth

BZK Antiseptic Towelette by

Drug Labeling and Warnings

BZK Antiseptic Towelette by is a Otc medication manufactured, distributed, or labeled by JINHUA JINGDI MEDICAL SUPPLIES CO., LTD, JINHUA JINGDI MEDICAL SUPPLIES CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium Chloride, 0.13% w/v

DESCRIPTION

First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.

Not made with natural rubber latex.

INACTIVE INGREDIENT

Sodium bicarbonate, purified water

PURPOSE

Antiseptic.

First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.

WARNINGS

For external use only.

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Directions

Clean the affected area.

DO NOT USE

Do not use in the eyes or over large areas of the body.

Ask a doctor before use if you have deep or puncture wounds or serious burns.

STOP USE

Stop use and ask a doctor if condition persists or gets worse.

DOSAGE & ADMINISTRATION

Apply topically as needed to cleanse intendend area；
Apply the product to the skin, take the injection or puncture site as the center, slowly rotate from the insideto the outside, and gradually apply the product for two times, the disinfection area should be more than5cmx5cm, and the action time should be 1min.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BZK ANTISEPTIC TOWELETTE 
benzalkonium chloride cloth cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83446-201
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 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83446-201-01	10000 in 1 CARTON	12/28/2025
1		1.5 g in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/28/2025

Labeler - JINHUA JINGDI MEDICAL SUPPLIES CO., LTD (546604382)

Registrant - JINHUA JINGDI MEDICAL SUPPLIES CO.,LTD (546604382)

Establishment
Name	Address	ID/FEI	Business Operations
JINHUA JINGDI MEDICAL SUPPLIES CO.,LTD		546604382	manufacture(83446-201)