Hand Sanitizer

Manufacturer: Allure Labs Inc
Effective date: 2020-11-25
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:34:25

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Wet hands thoroughly with product Allow to dry without wiping Not recommended for infants For children under 6, use only under adult supervision

Storage and handling

Store at room temperature Do not freeze May discolor certain fabrics or surfaces Do not store above 105 ºF

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65% w/w.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce microorganisms on the skin.
Recommended for repeat use.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rise eyes thouroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product
Allow to dry without wiping
Not recommended for infants
For children under 6, use only under adult supervision

Other information

STORAGE AND HANDLING SECTION

Store at room temperature
Do not freeze
May discolor certain fabrics or surfaces
Do not store above 105 ºF

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(aqua), Glycerin, Acrylates Copolymer, Sodium Hydroxide, Fragrance (parfum), Benzyl Benzoate, Citral, Geraniol, Hexyl Cinnamaldehyde, linalool

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand Sanitizer 65Birdzeyelabs.com

Dist. and sold by Birdzeye Labs, LLC

San Mateo, CA USA

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
902574	ethanol 65 % Topical Gel	PSN	1
902574	ethanol 0.65 ML/ML Topical Gel	SCD	1
902574	ethyl alcohol 65 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62742-4191-1	2023-01-30	C162847	48780-1	f386c649-f2ac-0266-e053-dadaa90a7c1a	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62742-4191-1	Hand Sanitizer	3785 mL in 1 BOTTLE	GEL	3785		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62742-4191	HAND SANITIZER (ETHYL ALCOHOL) GEL [ALLURE LABS INC]	1	Legacy NDC, 1 package rows	20201201_b4f9bc4f-9dca-090f-e053-2a95a90a07d9.zip

Products#

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

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

Hand Sanitizer
ETHYL ALCOHOL
.ALPHA.-HEXYLCINNAMALDEHYDE
BENZYL BENZOATE
CITRAL
GERANIOL
LINALOOL, (+/-)-
SODIUM HYDROXIDE
GLYCERIN
ACRYLATES CROSSPOLYMER-6
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62742-4191	62742-4191-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
.ALPHA.-HEXYLCINNAMALDEHYDE	7X6O37OK2I	IACT
BENZYL BENZOATE	N863NB338G	IACT
CITRAL	T7EU0O9VPP	IACT
GERANIOL	L837108USY	IACT
LINALOOL, (+/-)-	D81QY6I88E	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
GLYCERIN	PDC6A3C0OX	IACT
ACRYLATES CROSSPOLYMER-6	4GXD0Q3OS3	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
b4f9cca7-08b3-9da7-e053-2995a90a169a			b4f9bc4f-9dca-090f-e053-2a95a90a07d9	2020-11-25	Warnings	Exact identifier spl id: b4f9cca7-08b3-9da7-e053-2995a90a169a spl set id: b4f9bc4f-9dca-090f-e053-2a95a90a07d9

Reported adverse events (FAERS/openFDA)#

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