Purifying Hand Sanitizer

Manufacturer
Allure Labs Inc
Effective date
2020-04-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:08:28

Label at a glance#

ProductPurifying Hand 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: 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), Glycerin, Lavandula angustifolia (lavender) oil.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

True Botanicals

San Francisco, CA 94111

Hand SanitizerHand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
884783ethanol 65 % Topical SolutionPSN1
884783ethanol 0.65 ML/ML Topical SolutionSCD1
884783ethanol 65 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62742-4188-12022-01-28C16284748780-1d6a99b39-5674-a426-e053-dadaa90af4c2DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62742-4188-1Purifying Hand Sanitizer30 mL in 1 BOTTLE, PUMPLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62742-4188PURIFYING HAND SANITIZER (ETHYL ALCOHOL) LIQUID [ALLURE LABS INC]1Legacy NDC, 1 package rows20200429_72f3761a-b144-49fb-959f-01ab5f1f95d6.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62742-418862742-4188-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
LAVENDER OILZBP1YXW0H8IACT

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
fc5efc96-3ae9-448c-95c5-1e0539dd2b1d72f3761a-b144-49fb-959f-01ab5f1f95d62020-04-28WarningsExact identifier
spl id: fc5efc96-3ae9-448c-95c5-1e0539dd2b1d
spl set id: 72f3761a-b144-49fb-959f-01ab5f1f95d6

Reported adverse events (FAERS/openFDA)#

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