Ethanol

Manufacturer: Golden Leaf Energy
Effective date: 2020-06-19
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:19:20

Label at a glance#

ProductEthanol

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

Active ingredient - Ethanol

OTC - ACTIVE INGREDIENT SECTION

Ethanol

WARNINGS SECTION

DosageDrug Facts/Warnings

INDICATIONS & USAGE SECTION

IndicationsDrug Facts - Indications and usage

OTC - PURPOSE SECTION

Drug Facts - Purpose Purpose

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reachDrug Facts - Keep out of reach of children

INACTIVE INGREDIENT SECTION

Inactive IngredientsDrug Facts - Inactive Ingredients

DOSAGE & ADMINISTRATION SECTION

Drug Facts - Dosage Dosage

96% Ethanol - 1000L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1000 Ethanol 1000L- Ethanol

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79137-001-01	2022-01-28	C162847	48780-1	d6a99b39-f669-a426-e053-dadaa90af4c2	a902a3b0-a538-8e6b-e053-2a95a90a7d5d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79137-001-01	Ethanol	1 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK	LIQUID	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79137-001	ETHANOL LIQUID [GOLDEN LEAF ENERGY]	1	Legacy NDC, 1 package rows	20200628_a902a3b0-a538-8e6b-e053-2a95a90a7d5d.zip

Products#

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

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

Ethanol
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79137-001	79137-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	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
a9048423-5684-727d-e053-2a95a90a38cd			a902a3b0-a538-8e6b-e053-2a95a90a7d5d	2020-06-19	Warnings	Exact identifier spl id: a9048423-5684-727d-e053-2a95a90a38cd spl set id: a902a3b0-a538-8e6b-e053-2a95a90a7d5d

Reported adverse events (FAERS/openFDA)#

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