HAND SANITIZER

Manufacturer: HEB
Effective date: 2010-07-05
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:25:00

Label at a glance#

ProductHAND SANITIZER WITH MOISTURIZERS AND VITAMIN E

Active ingredientALCOHOL

Label structure5 sections

Indications and uses

USES: TO HELP REDUCE BACTERIA ON THE SKIN. DIRECTIONS: PUT A SMALL AMOUNT INTO YOUR PALM AND BRISKLY RUB HANDS TOGETHER UNTIL DRY.

Dosage and administration

USES: TO HELP REDUCE BACTERIA ON THE SKIN. DIRECTIONS: PUT A SMALL AMOUNT INTO YOUR PALM AND BRISKLY RUB HANDS TOGETHER UNTIL DRY.

Storage and handling

FLAMMABLE. KEEP AWAY FROM HEAT AND FLAME.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 62% (ANTISEPTIC)

USES AND DIRECTIONS

OTC - PURPOSE SECTION

USES: TO HELP REDUCE BACTERIA ON THE SKIN.
DIRECTIONS: PUT A SMALL AMOUNT INTO YOUR PALM AND BRISKLY RUB HANDS TOGETHER UNTIL DRY.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY.IN CASE OF ACCIDENTAL INGESTION, SEEK MEDICAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER. AVOID CONTACT WITH BROKEN SKIN.

STOP USE AND ASK A DOCTOR IF

OTC - STOP USE SECTION

SKIN IRRITATION OR REDNESS DEVELOPS.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

FOR CHILDREN UNDER 6, USE ONLY WITH ADULT SUPERVISION. NOT RECOMMENDED FOR USE ON INFANTS.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

FLAMMABLE. KEEP AWAY FROM HEAT AND FLAME.

PACKAGE FRONT AND BACK LABELS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

8OZ FRONT AND BACK LABELS: HCF8OZ.jpg8OZ FRONT AND BACK LABELS

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	1
581660	ethanol 0.62 ML/ML Topical Gel	SCD	1
581660	ethanol 62 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
37808-225-08	2020-01-31	C162847	48780-1	9d75b9d0-2086-f424-e053-dadaa90a57ce	BACK LABEL - DRUG FACTS BOX

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
37808-225-08	HAND SANITIZERWITH MOISTURIZERS AND VITAMIN E	237 mL in 1 BOTTLE, PUMP	GEL	237		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
37808-225	HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E (ETHYL ALCOHOL) GEL [HEB]	1	Legacy NDC, 1 package rows	20100706_4d8c8a94-98fe-41ce-b010-504b87c31292.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
ALCOHOL	ACTIVE INGREDIENT	3K9958V90M	1
ALCOHOL	ACTIVE MOIETY	3K9958V90M	1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E
ETHYL ALCOHOL
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
37808-225	37808-225-08

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
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
0faef1c4-1af2-4b9b-a44d-8d2914a4392f			4d8c8a94-98fe-41ce-b010-504b87c31292	2010-07-05	Warnings	Exact identifier spl id: 0faef1c4-1af2-4b9b-a44d-8d2914a4392f spl set id: 4d8c8a94-98fe-41ce-b010-504b87c31292

Reported adverse events (FAERS/openFDA)#

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