FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
INTENTLY (GUANGZHOU) BIOTECHNOLOGY CO., LTD.
Effective date
2020-06-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:33

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Store between 15-30°C(59-86°F)

Avoid feezing and excessive heat above40°C (104°F)

INACTIVE INGREDIENT SECTION

Water

Glycerin

Hydrogen Peroxide

Tert-butyl alcohol

Denatonium benzoate

INDICATIONS & USAGE SECTION

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

OTC - ACTIVE INGREDIENT SECTION

Ethanol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

For external use only.Flammable. Keep away from heat or flame.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130376885999990GTIN-13: 0376885999990
EAN-13: 0376885999990
GTIN-12: 376885999990
UPC-A: 376885999990
GTIN storage (14 digits): 00376885999990		label.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55467-010-012022-01-28C16284748780-1d6a99b39-da28-a426-e053-dadaa90af4c2a70104a0-1bae-3a7e-e053-2995a90a6f42

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55467-010-01Hand Sanitizer30 mL in 1 BOTTLEGEL301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55467-010HAND SANITIZER GEL [INTENTLY (GUANGZHOU) BIOTECHNOLOGY CO., LTD.]1Legacy NDC, 1 package rows20200601_a70104a0-1bae-3a7e-e053-2995a90a6f42.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55467-01055467-010-01

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
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
GLYCERINPDC6A3C0OXIACT
TERT-BUTYL ALCOHOLMD83SFE959IACT
DENATONIUM BENZOATE4YK5Z54AT2IACT

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
a70104a0-1baf-3a7e-e053-2995a90a6f42a70104a0-1bae-3a7e-e053-2995a90a6f422020-06-01WarningsExact identifier
spl id: a70104a0-1baf-3a7e-e053-2995a90a6f42
spl set id: a70104a0-1bae-3a7e-e053-2995a90a6f42

Reported adverse events (FAERS/openFDA)#

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