HAND SANITIZER

Manufacturer: VIRGIN SCENT INC.
Effective date: 2020-04-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:06:57

Label at a glance#

ProductHAND SANITIZER

Active ingredientALCOHOL

Label structure6 sections

Indications and uses

HELPS REDUCE BACTERIA ON THE SKIN. RECOMMENDED FOR REPEATED USE.

Dosage and administration

DISPENSE ONE PUMP OF SANITIZER ONTO HANDS AND RUB TOGETHER UNTIL DRY. USE AS NEEDED. FOR CHILDREN UNDER 6, USE WITH ADULT SUPERVISION. NOT RECOMMENDED FOR INFANTS. STORE BELOW 110 (DEGREES FAHRENHEIT). MAY CAUSE DISCOLORATION TO CERTAIN FABRICS AND SURFACES.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 65%

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USES:

INDICATIONS & USAGE SECTION

HELPS REDUCE BACTERIA ON THE SKIN. RECOMMENDED FOR REPEATED USE.

WARNINGS:

WARNINGS SECTION

FOR EXTERNAL USE ONLY. FLAMMABLE. KEEP AWAY FROMFIRE OR FLAME.

WHEN USING THIS PRODUCT,

OTC - WHEN USING SECTION

AVOID CONTACT WITH EYES. IN CASE OF CONTACT WITH EYES, FLUSH THOROUGHLY WITH WATER. AVOID CONTACT WITH BROKEN SKIN.

STOP USE AND ASK DOCTOR

OTC - STOP USE SECTION

IF IRRITATION OR REDNESS DEVELOPS, OR IF CONDITION PERSISTS FOR MORE THAN 72 HOURS.

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

DISPENSE ONE PUMP OF SANITIZER ONTO HANDS AND RUB TOGETHER UNTIL DRY. USE AS NEEDED. FOR CHILDREN UNDER 6, USE WITH ADULT SUPERVISION. NOT RECOMMENDED FOR INFANTS.

OTHER INFO:

SPL UNCLASSIFIED SECTION

STORE BELOW 110 (DEGREES FAHRENHEIT). MAY CAUSE DISCOLORATION TO CERTAIN FABRICS AND SURFACES.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, ALOE BARBADENSIS LEAF EXTRACT, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ALCOHOL, TETRAHYDROXYPROPYL ETHYLENEDIAMINE

PACKAGE LABELING:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

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
74642-002-00	2023-01-30	C162847	48780-1	f386c64a-49ac-0266-e053-dadaa90a7c1a	HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74642-002-00	HAND SANITIZER	236 mL in 1 BOTTLE	GEL	236		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74642-002	HAND SANITIZER (ALCOHOL) GEL [VIRGIN SCENT INC.]	1	Legacy NDC, 1 package rows	20200420_a32f12a1-408c-738d-e053-2a95a90a6609.zip

Products#

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

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

HAND SANITIZER
ALCOHOL
WATER
ALOE VERA LEAF
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
EDETOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74642-002	74642-002-00

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
EDETOL	Q4R969U9FR	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
a32f1a0b-a9ef-883a-e053-2a95a90a8c12			a32f12a1-408c-738d-e053-2a95a90a6609	2020-04-13	Warnings	Exact identifier spl id: a32f1a0b-a9ef-883a-e053-2a95a90a8c12 spl set id: a32f12a1-408c-738d-e053-2a95a90a6609

Reported adverse events (FAERS/openFDA)#

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