ANGEL TREE HAND SANITIZER SPRAY, 62% ETHYL ALCOHOL, LAVENDER

Manufacturer: Angel Tree Products Inc.
Effective date: 2020-11-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:34:11

Label at a glance#

ProductHand Sanitizer Lavender

Active ingredientALCOHOL

Label structure10 sections

Dosage and administration

WET HANDS THOROUGHLY WITH THIS PRODUCT AND RUB LIGHTLY UNTIL DRY. DO NOT WIPE OFF OR RINSE.

Storage and handling

Store at room temperature Flammable, keep away from fire or flame.

Contacts and useful links#

PhonePoison Help(800) 222-1222

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 62% W/W

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on skin when water and soap are not available.

Warnings

WARNINGS SECTION

For external use only.

Do not use if you are allergic to any of the ingredients.
When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

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: (800) 222-1222

Directions

DOSAGE & ADMINISTRATION SECTION

WET HANDS THOROUGHLY WITH THIS PRODUCT AND RUB LIGHTLY UNTIL DRY. DO NOT WIPE OFF OR RINSE.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature
Flammable, keep away from fire or flame.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, GLYCERIN, LAVENDER OIL

Questions?

OTC - QUESTIONS SECTION

questions@angeltree.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Hand Sani Spray_4oz

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1020364	ethanol 62 % Topical Spray	PSN	1
1020364	ethanol 0.62 ML/ML Topical Spray	SCD	1
1020364	ethanol 62 % Topical Spray	SY	1
1020364	ethyl alcohol 62 % Topical Spray	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77890-101-14	2022-01-28	C162847	48780-1	d6a99b39-b454-a426-e053-dadaa90af4c2	ANGEL TREE HAND SANITIZER SPRAY, 62% ETHYL ALCOHOL, LAVENDER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77890-101-14	Hand SanitizerLavender	118.3 mL in 1 BOTTLE, SPRAY	SPRAY	118.3		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77890-101	HAND SANITIZER LAVENDER (ALCOHOL) SPRAY [ANGEL TREE PRODUCTS INC.]	1	Legacy NDC, 1 package rows	20201125_2dd0a728-1f53-4114-9995-a15ceaec4239.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Hand Sanitizer Lavender
Alcohol
WATER
GLYCERIN
LAVENDER OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77890-101	77890-101-14
66538-302

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
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
LAVENDER OIL	ZBP1YXW0H8	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
3c1328e2-fe39-48f3-b806-f35125ac7512			2dd0a728-1f53-4114-9995-a15ceaec4239	2020-11-24	Warnings	Exact identifier spl id: 3c1328e2-fe39-48f3-b806-f35125ac7512 spl set id: 2dd0a728-1f53-4114-9995-a15ceaec4239

Reported adverse events (FAERS/openFDA)#

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