(QIQING) SKIN DISINFECTANT- benzethonium chloride liquid

(Qiqing) Skin Disinfectant by

Drug Labeling and Warnings

(Qiqing) Skin Disinfectant by is a Otc medication manufactured, distributed, or labeled by QINGDAO PRECISION MEDICAL TECHNOLOGY CO.,LTD. ZIBO BRANCH. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzethonium Chloride 1.80g / L ± 10%

PURPOSE

Antibacterial

WARNINGS

1. This product is an external disinfectant.Prohibition of oral administration. Keep it out of reach of children.

2. Avoid contact with organics and antagonists. Do not use with soap or other anionic detergents, nor use with iodine or peroxides (such as potassium permanganate, hydrogen peroxide, sulfa powder, etc.).

WHEN USING

Avoid contact with organics and antagonists. Do not use with soap or other anionic detergents, nor use with iodine or peroxides (such as potassium permanganate, hydrogen peroxide, sulfa powder, etc.).

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

INACTIVE INGREDIENT

Allantoin, Water

DOSAGE & ADMINISTRATION

Topical Liquid

INDICATIONS & USAGE

For handwashing to decrease bacteria on the skin

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

(QIQING) SKIN DISINFECTANT 
benzethonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77919-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	1.8 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALLANTOIN (UNII: 344S277G0Z)	2 g  in 1000 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77919-002-01	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/21/2020
2	NDC: 77919-002-02	50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/21/2020
3	NDC: 77919-002-03	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/21/2020
4	NDC: 77919-002-04	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/21/2020
5	NDC: 77919-002-05	250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/21/2020
6	NDC: 77919-002-06	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/21/2020
7	NDC: 77919-002-07	750 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/21/2020
8	NDC: 77919-002-08	1000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/21/2020
9	NDC: 77919-002-09	1500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/21/2020
10	NDC: 77919-002-10	2000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/21/2020

Labeler - QINGDAO PRECISION MEDICAL TECHNOLOGY CO.,LTD. ZIBO BRANCH (554534589)

Registrant - QINGDAO PRECISION MEDICAL TECHNOLOGY CO.,LTD. ZIBO BRANCH (554534589)

Establishment
Name	Address	ID/FEI	Business Operations
QINGDAO PRECISION MEDICAL TECHNOLOGY CO.,LTD. ZIBO BRANCH		554534589	manufacture(77919-002)