Ethyl Rubbing Alcohol

Manufacturer: P & L Development, LLC
Effective date: 2019-04-09
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: legacy-cache
Hydrated at: 2026-08-02 00:26:21

Label at a glance#

ProductEthyl Rubbing Alcohol

Active ingredientALCOHOL

Label structure12 sections

Indications and uses

first aid to help prevent the risk of infection in minor cuts, scrapes and burns

Dosage and administration

clean affected area apply small amount of this product on the area 1-3 times daily may be covered with a small bandage If bandaged, let dry first

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol (70 percent concentration)

Purpose

OTC - PURPOSE SECTION

first aid antiseptic

Uses

INDICATIONS & USAGE SECTION

first aid to help prevent the risk of infection in minor cuts, scrapes and burns

Warnings

WARNINGS SECTION

for external use only

flammable, keep away from fire or flame

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

deep or puncture wounds, animal bites or serious burns

When using this product

OTC - WHEN USING SECTION

do not get into eyes

do not apply over large areas of the body

do not use longer than one week unless directed by a doctor

Stop use and ask a doctor if

OTC - STOP USE SECTION

conditions persists or gets worse

Keep this and all drugs out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion seek professional assistance, or contact a poison control center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

clean affected area

apply small amount of this product on the area 1-3 times daily

may be covered with a small bandage

If bandaged, let dry first

Other Information

SPL UNCLASSIFIED SECTION

store at controlled room temperature

will produce serious gastric disturbances if taken internally

Inactive Ingredient

INACTIVE INGREDIENT SECTION

acetone, denatonium benzoate, methyl isobutyl ketone, purified water

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aaron Brands

Ethyl

Rubbing Alcohol

70% by Volume

16 FL OZ (1 PT.) 473 mL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ALCOHOL	ACTIVE INGREDIENT	3K9958V90M	1
ALCOHOL	ACTIVE MOIETY	3K9958V90M	1
ACETONE	INACTIVE INGREDIENT	1364PS73AF	1
DENATONIUM BENZOATE	INACTIVE INGREDIENT	4YK5Z54AT2	1
METHYL ISOBUTYL KETONE	INACTIVE INGREDIENT	U5T7B88CNP	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Ethyl Rubbing Alcohol
ALCOHOL
WATER
ACETONE
METHYL ISOBUTYL KETONE
DENATONIUM BENZOATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49580-0905	49580-0905-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
ACETONE	1364PS73AF	IACT
METHYL ISOBUTYL KETONE	U5T7B88CNP	IACT
DENATONIUM BENZOATE	4YK5Z54AT2	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Match
DENATONIUM BENZOATE	DENATONIUM BENZOATE	4YK5Z54AT2	SWAB / TOPICAL	NA	Exact identifier — unii candidate 3 equally ranked IID candidates
DENATONIUM BENZOATE	DENATONIUM BENZOATE	4YK5Z54AT2	GEL / TOPICAL	NA	Exact identifier — unii candidate 3 equally ranked IID candidates
ACETONE	ACETONE	1364PS73AF	TABLET, EXTENDED RELEASE / ORAL	NA	Exact identifier — unii candidate
DENATONIUM BENZOATE	DENATONIUM BENZOATE	4YK5Z54AT2	SOLUTION / TOPICAL	NA	Exact identifier — unii candidate 3 equally ranked IID candidates

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
defae55e-fecc-4418-b5c5-a9bcb1b2adc4			56ee086e-128f-41a2-af27-d5e93fa91e54	2019-04-09	Warnings	Exact identifier spl id: defae55e-fecc-4418-b5c5-a9bcb1b2adc4 spl set id: 56ee086e-128f-41a2-af27-d5e93fa91e54

Reported adverse events (FAERS/openFDA)#

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