YOUKE AN- benzalkonium chloride disinfectant spray liquid

Youke an by

Drug Labeling and Warnings

Youke an by is a Otc medication manufactured, distributed, or labeled by HUNAN ZONWE PHARMACEUTICAL CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

benzalkonium chloride

KEEP OUT OF REACH OF CHILDREN

keep out of children

PURPOSE

Kills 99.99% of germs

DOSAGE & ADMINISTRATION

a little

INDICATIONS & USAGE

It shall be directly sprayed onto skin, wounds, mucosa and infected parts. It can be applied several times a day to bring continuous antiseptic effects on skin surface for lasting protection.

INACTIVE INGREDIENT

Propylene glycol

Sodium dihydrogen phosphate dihydrate

Disodium hydrogen phosphate

Disodium edetate, dihydrate

water

WARNINGS

1.This product is one kind of solution for external use, and is never for internal usage.
2.Activity of this product may be affected by anion surfactant or soap, and cannot be used together.
3.It is forbidden for people who are allergic to this product.
4.Turbidity or deposits may appear at a low temperature. It can be placed in warm waterfor heating, or used after it is dissolved through shaking.
5.It shall be sealed and kept in a dark and dry place.
6.Mucosa disinfection is only used for diagnosis and treatment by a medical institution.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

YOUKE AN 
benzalkonium chloride disinfectant spray liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54749-001
Route of Administration	EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM (UNII: 7N6JUD5X6Y) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM	0.072 mg  in 60 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)
SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white (transparent)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54749-001-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/06/2020

Labeler - Hunan Zhongwei Pharmaceutical Co., Ltd (547493962)

Establishment
Name	Address	ID/FEI	Business Operations
Hunan Zhongwei Pharmaceutical Co., Ltd		547493962	manufacture(54749-001)