ETHYL ALCOHOL

Manufacturer: ASP Global, LLc
Effective date: 2021-11-22
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 22:25:55

Label at a glance#

ProductETHYL ALCOHOL

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

Apply topically as needed to clean intended area. Discard after single use.

Contacts and useful links#

Websitewww.aspglobal.com

www.aspglobal.com

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for preparation of the skin prior to an injection.

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away from fire or flame. Do not use with electrocautery procedures or near eyes. Stop use and ask a doctor if irritation or redness develops.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply topically as needed to clean intended area. Discard after single use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Benzethonium Chloride, IPBC

PRINCIPAL DISPLAY PANEL - 80 Wipe Applicator Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ASP
MEDICAL

80 WIPES
REORDER #
WHS080
www.aspglobal.com

HAND SANITIZER
WIPES
Unscented • 75% Alcohol

Single Use
Not Made With
Natural Rubber Latex

OPEN

PRINCIPAL DISPLAY PANEL - 80 Wipe Applicator Package

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
59448-009-01	2022-07-29	C162847	48780-1	e4f33bdf-aee1-d8a0-e053-dadaa90a6e4e	ETHYL ALCOHOL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59448-009	ETHYL ALCOHOL (ALCOHOL) CLOTH [ASP GLOBAL, LLC]	2	Legacy NDC	20211125_77838d08-21db-494c-ac1b-e4155d4423bc.zip

Products#

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

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

ETHYL ALCOHOL
ALCOHOL
Benzethonium Chloride
Water
IODOPROPYNYL BUTYLCARBAMATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59448-009	59448-009-01

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
Benzethonium Chloride	PH41D05744	IACT
Water	059QF0KO0R	IACT
IODOPROPYNYL BUTYLCARBAMATE	603P14DHEB	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
f54b2609-41d6-42a8-890d-916d0b931296			77838d08-21db-494c-ac1b-e4155d4423bc	2025-12-23	Warnings	Exact identifier spl set id: 77838d08-21db-494c-ac1b-e4155d4423bc

Reported adverse events (FAERS/openFDA)#

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