Hand Sanitizer

Manufacturer: Allure Labs Inc
Effective date: 2021-02-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:38:21

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

Helps to reduce bacteria on the skin. For repeat use.

Dosage and administration

Apply all over your hands and allow to dry. Do not rinse off. For children under 6, use only under adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses:

INDICATIONS & USAGE SECTION

Helps to reduce bacteria on the skin. For repeat use.

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away from heat and flame. Do not store above 104ºF/40ºC.

OTC - WHEN USING SECTION

When using this product

• 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 immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

Apply all over your hands and allow to dry. Do not rinse off. For children under 6, use only under adult supervision. Not recommended for infants.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Glycerin, Aloe Barbadensis (Aloe Vera) Leaf Juice*, Pinus Sylvestris Leaf (Nordic Pine) Oil, Eucalyptus Globulus Leaf Oil*, Rosmarinus Officinalis (Rosemary) Oil, Linalool, Limonene.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aevi Wellness, Inc
251 Little Falls Drive
Wilmington, DE 19808
Made in USA

IMGAVHS

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62742-4201-1	2023-01-30	C162847	48780-1	f386c649-ea41-0266-e053-dadaa90a7c1a	Drug Facts
62742-4201-2	2023-01-30	C162847	48780-1	f386c649-ea41-0266-e053-dadaa90a7c1a	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62742-4201-1	Hand Sanitizer	237 mL in 1 BOTTLE	GEL	237		1
62742-4201-2	Hand Sanitizer	59 mL in 1 BOTTLE	GEL	59		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62742-4201	HAND SANITIZER (ETHYL ALCOHOL) GEL [ALLURE LABS INC]	1	Legacy NDC, 2 package rows	20210220_bba6701f-b164-969a-e053-2a95a90a25b9.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

Hand Sanitizer
Ethyl Alcohol
ALCOHOL
GLYCERIN
EUCALYPTUS OIL
PINE NEEDLE OIL (PINUS SYLVESTRIS)
ROSMARINUS OFFICINALIS FLOWERING TOP OIL
LIMONENE, (+)-
WATER
ALOE VERA LEAF
LINALOOL, (+/-)-

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62742-4201	62742-4201-1, 62742-4201-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
EUCALYPTUS OIL	2R04ONI662	IACT
PINE NEEDLE OIL (PINUS SYLVESTRIS)	5EXL5H740Y	IACT
ROSMARINUS OFFICINALIS FLOWERING TOP OIL	OXN0D3N28L	IACT
LIMONENE, (+)-	GFD7C86Q1W	IACT
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
LINALOOL, (+/-)-	D81QY6I88E	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
bba6701f-b165-969a-e053-2a95a90a25b9			bba6701f-b164-969a-e053-2a95a90a25b9	2021-02-18	Warnings	Exact identifier spl id: bba6701f-b165-969a-e053-2a95a90a25b9 spl set id: bba6701f-b164-969a-e053-2a95a90a25b9

Reported adverse events (FAERS/openFDA)#

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