FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Allure Labs Inc
Effective date
2020-04-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:35

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Ethyl Alcohol - 70%

OTC - PURPOSE SECTION

Purpose: Antimicrobial

INDICATIONS & USAGE SECTION

Uses: Helps to reduce bacteria on skin. Recommended for repeated use.

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.
  • Avoid contact with broken skin.

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), Acrylates Copolymer, Glycerin, Sodium Hydroxide.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MANUFACTURED FOR

ECZEMA HONEY CO BY,

ALLURE LABS,

HAYWARD, CA, 94545

Hand SanitizerHand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62742-4187-12022-01-28C16284748780-1d6a99b39-6f97-a426-e053-dadaa90af4c2DRUG FACTS
62742-4187-22022-01-28C16284748780-1d6a99b39-6f97-a426-e053-dadaa90af4c2DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62742-4187-1Hand Sanitizer59 mL in 1 BOTTLE, PUMPGEL591
62742-4187-2Hand Sanitizer237 mL in 1 BOTTLE, PUMPGEL2371

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62742-4187HAND SANITIZER (ETHYL ALCOHOL) GEL [ALLURE LABS INC]1Legacy NDC, 2 package rows20200424_a0f3e414-210f-4265-bb45-c4420bf40693.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
62742-418762742-4187-1, 62742-4187-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT
GLYCERINPDC6A3C0OXIACT
SODIUM HYDROXIDE55X04QC32IIACT

Source Document#

Source XML · Source PDF

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
6838ced3-e92b-4334-8622-44115228c172a0f3e414-210f-4265-bb45-c4420bf406932020-04-23WarningsExact identifier
spl id: 6838ced3-e92b-4334-8622-44115228c172
spl set id: a0f3e414-210f-4265-bb45-c4420bf40693

Reported adverse events (FAERS/openFDA)#

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