FDA.reportPublic FDA data

ETHYL ALCOHOL 80 PERCENT

Manufacturer
BEARCO
Effective date
2020-06-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:19:06

Label at a glance#

ProductETHYL ALCOHOL 80 PERCENT
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE ADMINISTRATION INFORAMTION - ETHYL ALCOHOL 80 PERCENT ANTISEPTIC

DOSAGE & ADMINISTRATION SECTION

DOSAGE & ADMINISTRATION INFODOSAGE & ADMINISTRATION INFO

WARNINGS INFORMATION - ETHYL ALCOHOL 80 PERCENT ANTISEPTIC

WARNINGS SECTION

WARNING INFORMATIONWARNING INFORMATION

INACTIVE INGREDIENTS - ETHYL ALCOHOL 80 PERCENT ANTISEPTIC

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS INFOINACTIVE INGREDIENTS INFO

INDICATIONS & USAGE INFORAMTION - ETHYL ALCOHOL 80 PERCENT ANTISEPTIC

INDICATIONS & USAGE SECTION

INDICATIONS/USAGEINDICATIONS/USAGE

ACTIVE INGREDIENT - ETHYL ALCOHOL 80 PERCENT ANTISEPTIC

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTACTIVE INGREDIENT

KEEP OUT OF REACH CHILDREN WARNING - ETHYL ALCOHOL 80 PERCENT ANTISEPTIC

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH CHILDRENKEEP OUT OF REACH CHILDREN

USE PURPOSE - ETHYL ALCOHOL 80 PERCENT ANTISEPTIC

OTC - PURPOSE SECTION

USE PURPOSEUSE PURPOSE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

750 mL Ethyl Alcohol 8- %750 mL Ethyl Alcohol 8- %

750 mL NDC 74331-800-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74331-800-012022-01-28C16284748780-1d6a99b39-8fc1-a426-e053-dadaa90af4c2ETHYL ALCOHOL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74331-800-01ETHYL ALCOHOL 80 PERCENT750 mL in 1 BOTTLELIQUID7501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74331-800ETHYL ALCOHOL 80 PERCENT (ETHYL ALCOHOL) LIQUID [BEARCO]1Legacy NDC, 1 package rows20200626_a8db4728-5284-5b27-e053-2a95a90ada5e.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74331-80074331-800-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
DENATONIUM BENZOATE4YK5Z54AT2IACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a8db4728-5285-5b27-e053-2a95a90ada5ea8db4728-5284-5b27-e053-2a95a90ada5e2020-06-24WarningsExact identifier
spl id: a8db4728-5285-5b27-e053-2a95a90ada5e
spl set id: a8db4728-5284-5b27-e053-2a95a90ada5e

Reported adverse events (FAERS/openFDA)#

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