aloe vera hand sanitizer

Manufacturer
XIAMEN EASEPAL ENTERPRISES LIMITED
Effective date
2020-03-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:04:20

Label at a glance#

Productaloe vera hand sanitizer handsanttizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

Flammable. Keep away from fire or flame.

INDICATIONS & USAGE SECTION

Directions. Put enough product in your palm to cover your hands completely. Rub hands together, covering all surfaces for approx. 25 seconds or until your hands are dry. Children under 6 years of age should be supervised when using this product.

DOSAGE & ADMINISTRATION SECTION

Store at 60'°F to 77°F (16°C to 25°C).

May discolor certain fabrics or surfaces.

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Triethanolamine.

Fragrance(Parfum) Lemon, Aloe Barbadensis Leaf Extract

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65.00%..

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
902574ethanol 65 % Topical GelPSN2
902574ethanol 0.65 ML/ML Topical GelSCD2
902574ethyl alcohol 65 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67984-001-012021-07-23C16284748780-1c7ccaba7-2157-fd44-e053-dadaa90aa01ba1abd16d-7dc5-a431-e053-2995a90a0c41

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67984-001-01aloe vera hand sanitizerhandsanttizer90 mL in 1 BOTTLEGEL902

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67984-001ALOE VERA HAND SANITIZER HANDSANTTIZER (HANDSANTTIZER) GEL [XIAMEN EASEPAL ENTERPRISES LIMITED]2Legacy NDC, 1 package rows20200331_a1abd16d-7dc5-a431-e053-2995a90a0c41.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67984-00167984-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
a214b45e-84f9-9e54-e053-2995a90a581ca1abd16d-7dc5-a431-e053-2995a90a0c412020-03-30WarningsExact identifier
spl id: a214b45e-84f9-9e54-e053-2995a90a581c
spl set id: a1abd16d-7dc5-a431-e053-2995a90a0c41

Reported adverse events (FAERS/openFDA)#

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