FDA.reportPublic FDA data

Gel Hand Sanitizer

Manufacturer
NA Chemical Inc
Effective date
2020-04-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:36:55

Label at a glance#

ProductGel Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

OTHER INFORMATION: Store above 32°F

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT: Denatured Ethanol 65%

OTC - PURPOSE SECTION

PURPOSE: Antiseptic

INDICATIONS & USAGE SECTION

USES: Hand sanitizer to help reduce bacteria on the skin.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Apply liberally to front and back of hands. Rub until dry.

WARNINGS SECTION

WARNINGS: For external use only.

When using this product, avoid contact with eyes.

In the case of contact with eyes, immediately flush with clean water.

Stop use and see a doctor if redness and irritation appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek medical help or contact Poison Control Center immediately.

STORAGE AND HANDLING SECTION

OTHER INFORMATION: Store above 32°F

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Proprietary and water.

SPL UNCLASSIFIED SECTION

NATIONAL automotive chemical 

Non-sterile solution

www.nachemical.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73895-922-012022-02-02C16284748780-1d6a99b39-54f1-a426-e053-dadaa90af4c2Gel Hand Sanitizer
73895-922-012022-01-28C16284748780-1d6a99b39-54f1-a426-e053-dadaa90af4c2Gel Hand Sanitizer

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
73895-92273895-922-01

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
ALCOHOL3K9958V90MACTIB
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
bfcdee88-3790-4c0f-8249-5ab2300014616ca9d53b-c5be-4e22-a9d3-969f9b04c9602022-02-02WarningsExact identifier
spl set id: 6ca9d53b-c5be-4e22-a9d3-969f9b04c960

Reported adverse events (FAERS/openFDA)#

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