Ethyl Rubbing Alcohol

Manufacturer: Strategic Sourcing Services LLC
Effective date: 2019-10-18
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-02 00:06:56

Label at a glance#

ProductEthyl Rubbing Alcohol

Active ingredientALCOHOL

Label structure10 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 sterile bandage If bandaged, let dry first

Contacts and useful links#

PhonePoison Help1-800-222-1222

Websitewww.sunmarkbrand.com

www.sunmarkbrand.com

Label contents#

Full prescribing information#

Active Ingredient (by volume)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol (70% conc.)

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
if taken internally serious gastric disturbances will result

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 out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of ingestion, get medical help or contact a poison control center (1-800-222-1222) 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 sterile bandage

If bandaged, let dry first

Other Information

SPL UNCLASSIFIED SECTION

store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

acetone, denatonium benzoate, methyl isobutyl ketone, purified water

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-8777-753-3935 Monday-Friday 9AM-5PM EST

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ethyl Rubbing Alcohol

70% USP

First aid antiseptic to help prevent infection in minor cuts, scrapes & burns

Warning: Flammable, keep away from spark, heat or flame.

FL OZ (mL)

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY FOIL UNDER CAP IS BROKEN OR MISSING.

Another Quality Product Distributed by McKesson

One Post Street, San Francisco, CA 94104

www.sunmarkbrand.com

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sunmark Ethyl Alcohol 70%

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49348-003-38	ML - Milliliter	49348-003	30dcae0e-7913-4e8f-a313-7fe3e5610e69	1	2012-07-24

DailyMed Socrata Ingredients#

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

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
49348-003	49348-003-38

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
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
DENATONIUM BENZOATE	DENATONIUM BENZOATE	4YK5Z54AT2	GEL / TOPICAL	NA	Exact identifier — unii candidate 3 equally ranked IID candidates
DENATONIUM BENZOATE	DENATONIUM BENZOATE	4YK5Z54AT2	SWAB / 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
976ca4c6-63c5-4d65-bcf8-43a41c298b2c			cc4aa406-c705-49a9-a506-73b79ea27e59	2020-09-16	Warnings	Exact identifier spl set id: cc4aa406-c705-49a9-a506-73b79ea27e59

Reported adverse events (FAERS/openFDA)#

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