FDA.reportPublic FDA data

ANTIBACTERIAL HANDS-FREE Gel

Manufacturer
Guangzhou Yuncai Fine Chemical CO.LTD
Effective date
2020-04-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:08:30

Label at a glance#

ProductANTIBACTERIAL HANDS-FREE Gel
Active ingredientALCOHOL
Label structure5 sections

Dosage and administration

This product is for external use and should not be taken orally.It should be used with caution for people with alcohol allergy.It should be keep out of reach of children and sealed to avoid direct sunlight.

Label contents#

Full prescribing information#

MAIN ACTIVE INGREDIENTS AND CONTENT

OTC - ACTIVE INGREDIENT SECTION

Ethanol 75%(W/W)

Use

INDICATIONS & USAGE SECTION

Applicable to the hand

Directions

DOSAGE & ADMINISTRATION SECTION

This product is for external use and should not be taken orally.It should be used with caution for people

with alcohol allergy.It should be keep out of reach of children and sealed to avoid direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,acrylic(ester) /C10-30

alkanol acrylatecrosslinked polymer, triethanolamine.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500 ml label500 ml label50 ml label50 ml label100 ml label100 ml label250 ml label250 ml label300 ml label300 ml label1000 ml label1000 ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75212-001-012021-07-23C16284748780-1c7ccaba7-252f-fd44-e053-dadaa90aa01bANTIBACTERIAL HAND GEL
75212-001-022021-07-23C16284748780-1c7ccaba7-252f-fd44-e053-dadaa90aa01bANTIBACTERIAL HAND GEL
75212-001-032021-07-23C16284748780-1c7ccaba7-252f-fd44-e053-dadaa90aa01bANTIBACTERIAL HAND GEL
75212-001-042021-07-23C16284748780-1c7ccaba7-252f-fd44-e053-dadaa90aa01bANTIBACTERIAL HAND GEL
75212-001-052021-07-23C16284748780-1c7ccaba7-252f-fd44-e053-dadaa90aa01bANTIBACTERIAL HAND GEL
75212-001-062021-07-23C16284748780-1c7ccaba7-252f-fd44-e053-dadaa90aa01bANTIBACTERIAL HAND GEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75212-001-01ANTIBACTERIAL HANDS-FREE Gel50 mL in 1 BOTTLEGEL502
75212-001-02ANTIBACTERIAL HANDS-FREE Gel100 mL in 1 BOTTLEGEL1002
75212-001-03ANTIBACTERIAL HANDS-FREE Gel250 mL in 1 BOTTLEGEL2502
75212-001-04ANTIBACTERIAL HANDS-FREE Gel300 mL in 1 BOTTLEGEL3002
75212-001-05ANTIBACTERIAL HANDS-FREE Gel1000 mL in 1 BOTTLEGEL10002
75212-001-06ANTIBACTERIAL HANDS-FREE Gel500 mL in 1 BOTTLEGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75212-001ANTIBACTERIAL HANDS-FREE GEL GEL [GUANGZHOU YUNCAI FINE CHEMICAL CO.LTD]2Legacy NDC, 6 package rows20200429_a352d09c-ee41-b009-e053-2a95a90a3940.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75212-00175212-001-01, 75212-001-02, 75212-001-03, 75212-001-04, 75212-001-06, 75212-001-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT

Source Document#

Source XML · Source PDF

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
a4025f4b-2300-028e-e053-2a95a90a253fa352d09c-ee41-b009-e053-2a95a90a39402020-04-24WarningsExact identifier
spl id: a4025f4b-2300-028e-e053-2a95a90a253f
spl set id: a352d09c-ee41-b009-e053-2a95a90a3940

Reported adverse events (FAERS/openFDA)#

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