FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Allure Labs Inc
Effective date
2020-03-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:01

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Ethyl Alcohol - 65%

OTC - PURPOSE SECTION

Purpose: Antimicrobial

INDICATIONS & USAGE SECTION

Uses: To decrease the risk of skin infection in minor cuts, scrapes and burns.

WARNINGS SECTION

Warning: For External use only - Hands

Flammable: Keep away from heat and Flame

OTC - WHEN USING SECTION

When using this products:

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation develops. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children:

  • If product is swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions:

  • Wet hands throughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water (Aqua), Glycerin, Carbomer, Triethanolamine, Fragrance (Parfume), Benzyl Benzoate, Citral, Geraniol, Hexyl Cinnam Aldehyde, Limonene, Lonalool.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Manufactured By

Allure Labs, Inc.

Hayward, CA 94544

www.allurelabs.com

ImageHandSanitImageHandSanit

ImageHandSanitImageHandSanit

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
902574ethanol 65 % Topical GelPSN1
902574ethanol 0.65 ML/ML Topical GelSCD1
902574ethyl alcohol 65 % Topical GelSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62742-4184-12022-01-28C16284748780-1d6a99b39-bb5f-a426-e053-dadaa90af4c2DRUG FACTS
62742-4184-22022-01-28C16284748780-1d6a99b39-bb5f-a426-e053-dadaa90af4c2DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62742-4184-1Hand Sanitizer59.14 mL in 1 BOTTLE, PUMPGEL59.141
62742-4184-2Hand Sanitizer355 mL in 1 BOTTLE, PUMPGEL3551

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62742-4184HAND SANITIZER (ETHYL ALCOHOL) GEL [ALLURE LABS INC]1Legacy NDC, 2 package rows20200319_0a087ec3-b12f-4035-b75a-f7d92b7b3fcf.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62742-418462742-4184-1, 62742-4184-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER 9404Q93RCW27EIACT
TROLAMINE9O3K93S3TKIACT
BENZYL BENZOATEN863NB338GIACT
CITRALT7EU0O9VPPIACT
GERANIOLL837108USYIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
LIMONENE, (+)-GFD7C86Q1WIACT
LINALOOL, (+/-)-D81QY6I88EIACT

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
a8b0ba79-3c72-4fe0-9605-baada50cb63a0a087ec3-b12f-4035-b75a-f7d92b7b3fcf2020-03-17WarningsExact identifier
spl id: a8b0ba79-3c72-4fe0-9605-baada50cb63a
spl set id: 0a087ec3-b12f-4035-b75a-f7d92b7b3fcf

Reported adverse events (FAERS/openFDA)#

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