BZK ANTISEPTIC TOWELETTE- benzalkonium chloride swab

BZK ANTISEPTIC TOWELETTE by

Drug Labeling and Warnings

BZK ANTISEPTIC TOWELETTE by is a Otc medication manufactured, distributed, or labeled by Yinjing Medical Technology (Shanghai) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride, 0.13% w/v

Purpose

First Aid Antiseptic

Use

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

Warnings

For external use only.

Do not use

• in the eyes or apply over large areas of the body
• longer than 1 week unless directed by a doctor.
  

Consult a doctor

in case of deep or puncture wounds, animal bites, or serious burns.

Stop use and 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

• Clean the affected area
• Apply a small amount of this product on the area 1 to 3 times daily
• May be covered with a sterile bandage when dry
  

Inactive ingredients

purified water, sodium bicarbonate

SPL UNCLASSIFIED SECTION

Shanghai Yinjing Medical Supplies Co., Ltd.
586 Yuanxi RD.Nanhui Industry Park,Shanghai 201300
Tel:+86-21-6801-6511  Http://www.yinjing.cn
E-mail: zhl@yinjing.cn
Made in China
LOT

PRINCIPAL DISPLAY PANEL

NDC：44019-323-01

inin      1 pad/pouch

BZK ANTISEPTIC TOWELETTE

For External Use Only

Product Label

INGREDIENTS AND APPEARANCE

BZK ANTISEPTIC TOWELETTE  
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44019-323
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

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: 44019-323-01	1 in 1 POUCH	08/03/2016
1		1.5 g in 1 PATCH; 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 not final	part333A	08/03/2016

Labeler - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)

Registrant - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)