Hand-washing antibacterial gel

Manufacturer
Hangzhou Tuojie Biotechnology Co.,Ltd.
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:38

Label at a glance#

ProductHand-washing antibacterial gel
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Airtight / dark storage

INACTIVE INGREDIENT SECTION

carbomer, triethanolamine, aloe extract, glycerin, deionized water

INDICATIONS & USAGE SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.

OTC - ACTIVE INGREDIENT SECTION

75% ethanol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

1. This product is an external product and should not be taken orally;
2. Those who are allergic to alcohol should use it with aution;
3. Airtight / dark storage;
4. This product is flammable and should be kept away from the fire source.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62178-001-012022-01-28C16284748780-1d6a99b39-cf85-a426-e053-dadaa90af4c2a78ccb78-8a29-605e-e053-2995a90a87d0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62178-001-01Hand-washing antibacterial gel250 mL in 1 BOTTLELIQUID2501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62178-001HAND-WASHING ANTIBACTERIAL GEL (HAND-WASHING ANTIBACTERIAL) LIQUID [HANGZHOU TUOJIE BIOTECHNOLOGY CO.,LTD.]1Legacy NDC, 1 package rows20200609_a78ccb78-8a29-605e-e053-2995a90a87d0.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62178-00162178-001-01

Ingredients#

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

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

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
a78ccb78-8a2a-605e-e053-2995a90a87d0a78ccb78-8a29-605e-e053-2995a90a87d02020-06-08WarningsExact identifier
spl id: a78ccb78-8a2a-605e-e053-2995a90a87d0
spl set id: a78ccb78-8a29-605e-e053-2995a90a87d0

Reported adverse events (FAERS/openFDA)#

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