ETHYL ALCOHOL

Manufacturer: PSS World Medical, Inc.
Effective date: 2010-04-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:24:17

Label at a glance#

ProductETHYL ALCOHOL

Active ingredientALCOHOL

Label structure6 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Select medical products Instant Hand Sanitizer

INDICATIONS & USAGE SECTION

DIRECTIONS:
Place enough product in your palm to thoroughly cover your hands
Rub hands together briskly until dry
Children under 6 years of age should be supervised when using this product.

INACTIVE INGREDIENT SECTION

Inactive ingredients Water (Aqua), Isopropyl Alcohol, Diisopropyl Sebacate, Glycerin, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate, Aminomethyl Propanol, Carbomer, Fragrance (Parfum)

WARNINGS SECTION

Warnings
Flammable. Keep away from fire or flame.For external use only
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash appears and lasts
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose
Ethyl Alcohol 62% Antimicrobial

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottle

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
68345-652-17	2019-10-21	C162847	48780-1	956f9ecf-dd07-621f-e053-dbdaa90a74ad	2d96c725-9fee-41ec-b1ef-9672570a3cb2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68345-652-17	ETHYL ALCOHOL	503 mL in 1 BOTTLE, PUMP	GEL	503		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68345-652	ETHYL ALCOHOL (ALCOHOL) GEL [PSS WORLD MEDICAL, INC.]	1	Legacy NDC, 1 package rows	20100421_2d96c725-9fee-41ec-b1ef-9672570a3cb2.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 · 2 matching rows.

ETHYL ALCOHOL
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
68345-652	68345-652-17

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
b840ef53-f095-4d3d-a4d3-e773d1a5573a			2d96c725-9fee-41ec-b1ef-9672570a3cb2	2010-04-21	Warnings	Exact identifier spl id: b840ef53-f095-4d3d-a4d3-e773d1a5573a spl set id: 2d96c725-9fee-41ec-b1ef-9672570a3cb2

Reported adverse events (FAERS/openFDA)#

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