Antibacterial foam hand wash

Manufacturer
Wuxi Youjie Technology Co. LTD
Effective date
2020-04-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:08:23

Label at a glance#

ProductAntibacterial foam hand wash
Active ingredientBENZALKONIUM BROMIDE
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Store in a cool and dry place.

INACTIVE INGREDIENT SECTION

water

INDICATIONS & USAGE SECTION

After wetting your hands, put a proper amount of liquid soap in your hands, gently rub them for 2 minutes, and then rinse them with water.

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM BROMIDE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization

WARNINGS SECTION

1. This productis for extemaluse. Itis not allowed to be taken intemally.Keep it out of children's reach.
2. Do not use with peroxide. Store in a cool and dry place. If it gets into your eyes, please rinse with water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codewww.china-youjie.com/label.jpg
QR code linkQR Code2dcode.org/0106951515000112label.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54796-001-012022-01-28C16284748780-1d6a99b39-7060-a426-e053-dadaa90af4c2a456a006-3cb1-0c13-e053-2995a90ab8f2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54796-001-01Antibacterial foam hand wash450 g in 1 BOTTLELIQUID4501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54796-001ANTIBACTERIAL FOAM HAND WASH LIQUID [WUXI YOUJIE TECHNOLOGY CO. LTD]1Legacy NDC, 1 package rows20200428_a456a006-3cb1-0c13-e053-2995a90ab8f2.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54796-00154796-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM BROMIDE151T1GQ42DACTIB
WATER059QF0KO0RIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a456a006-3cb2-0c13-e053-2995a90ab8f2a456a006-3cb1-0c13-e053-2995a90ab8f22020-04-28WarningsExact identifier
spl id: a456a006-3cb2-0c13-e053-2995a90ab8f2
spl set id: a456a006-3cb1-0c13-e053-2995a90ab8f2

Reported adverse events (FAERS/openFDA)#

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