FDA.reportPublic FDA data

HAND WASH ANTIBACTERIAL

Manufacturer
Wuxi Yongning Daily Chemical Factory
Effective date
2020-03-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:22

Label at a glance#

ProductHAND WASH ANTIBACTERIAL
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

This product is a disinfectantfor external use and should not be taken orally.

Do not sterilize woundsand broken skin.

INACTIVE INGREDIENT SECTION

Carbomer glycerol Triethanolamine

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

OTC - ACTIVE INGREDIENT SECTION

ethanol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

Flammable, keep away from the source of fire.

INDICATIONS & USAGE SECTION

Evenly apply appropriate amount of this product to the hands and wipe for 1 minute.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54607-002-012022-01-28C16284748780-1d6a99b39-bc58-a426-e053-dadaa90af4c2a1faa0a9-e4c5-8b26-e053-2995a90ad7d2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54607-002-01HAND WASH ANTIBACTERIAL500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54607-002HAND WASH ANTIBACTERIAL GEL [WUXI YONGNING DAILY CHEMICAL FACTORY]1Legacy NDC, 1 package rows20200331_a1faa0a9-e4c5-8b26-e053-2995a90ad7d2.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54607-00254607-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT

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
a1faa0a9-e4c6-8b26-e053-2995a90ad7d2a1faa0a9-e4c5-8b26-e053-2995a90ad7d22020-03-29WarningsExact identifier
spl id: a1faa0a9-e4c6-8b26-e053-2995a90ad7d2
spl set id: a1faa0a9-e4c5-8b26-e053-2995a90ad7d2

Reported adverse events (FAERS/openFDA)#

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