Youke an

Manufacturer: HUNAN ZONWE PHARMACEUTICAL CO., LTD.
Effective date: 2020-11-20
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:33:56

Label at a glance#

ProductYouke an

Active ingredientBENZALKONIUM

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

benzalkonium chloride

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of children

OTC - PURPOSE SECTION

Kills 99.99% of germs

DOSAGE & ADMINISTRATION SECTION

a little

INDICATIONS & USAGE SECTION

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 SECTION

Propylene glycol

Sodium dihydrogen phosphate dihydrate

Disodium hydrogen phosphate

Disodium edetate, dihydrate

water

WARNINGS SECTION

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
54749-001-01	2022-01-28	C162847	48780-1	d6a99b39-64f9-a426-e053-dadaa90af4c2	a2a1ecde-fecf-3744-e053-2a95a90a4251

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
54749-001-01	Youke an	60 mL in 1 BOTTLE	LIQUID	60		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
54749-001	YOUKE AN (BENZALKONIUM CHLORIDE DISINFECTANT SPRAY) LIQUID [HUNAN ZONWE PHARMACEUTICAL CO., LTD.]	2	Legacy NDC, 1 package rows	20201120_a2a1ecde-fecf-3744-e053-2a95a90a4251.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

Youke an
Benzalkonium Chloride Disinfectant Spray
PROPYLENE GLYCOL
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE
SODIUM PHOSPHATE DIBASIC DIHYDRATE
WATER
BENZALKONIUM
EDETATE DISODIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
54749-001	54749-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PROPYLENE GLYCOL	6DC9Q167V3	IACT
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE	5QWK665956	IACT
SODIUM PHOSPHATE DIBASIC DIHYDRATE	94255I6E2T	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM	7N6JUD5X6Y	ACTIB
EDETATE DISODIUM	7FLD91C86K	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
b483dc16-b295-3646-e053-2a95a90a7f4a			a2a1ecde-fecf-3744-e053-2a95a90a4251	2020-11-20	Warnings	Exact identifier spl id: b483dc16-b295-3646-e053-2a95a90a7f4a spl set id: a2a1ecde-fecf-3744-e053-2a95a90a4251

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.