Ethyl Alcohol by Walmart Inc. / Consumer Product Partners, LLC ETHYL ALCOHOL liquid

Ethyl Alcohol by

Drug Labeling and Warnings

Ethyl Alcohol by is a Otc medication manufactured, distributed, or labeled by Walmart Inc., Consumer Product Partners, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl alcohol 70%

Purpose

First aid antiseptic

Uses

first aid to help prevent the risk of infection in:

• minor cuts
• scrapes
• burns

Warnings

For external use only.If taken internally serious gastric disturbances will result.

Flammable

• keep away from fire or flame, heat spark, electrical

Ask a doctor before use

for deep or puncture wounds, animal bites or serious burns

When using this product

• do not get into eyes
• do not inhale
• do not apply over large areas of the body
• do not use longer than 1 week

Stop use and ask a doctor if

condition persists or gets worse

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Caution

Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product.

Directions

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

Inactive ingredients

acetone, denatonium benzoate, methyl isobutyl ketone, water

Questions or comments?

1-800-287-1915

Adverse event

DSP-TN-21091 DSP-MO-20087

DISTRIBUTED BY: Walmart, Inc., Bentonville, AR 72718

Pat. D675,101

PRINCIPAL DISPLAY PANEL

NDC: 79903-283-32

equate™

Ethyl Rubbing Alcohol

70% by volume

First Aid Antiseptic

WARNING FLAMMABLE - Keep away from heat, spark, electrical, fire or flame

Use only in a well-ventilated are; fumes can be harmful.

CAUTION: Do not point at self or others; product will squirt when squeezed.

Discard Seal, Empty, & Replace Cap

PLASTIC BOTTLE

how2recycle.info

32 FL OZ (1 QT) 946 mL

INGREDIENTS AND APPEARANCE

ETHYL ALCOHOL 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-283
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ACETONE (UNII: 1364PS73AF)
WATER (UNII: 059QF0KO0R)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
METHYL ISOBUTYL KETONE (UNII: U5T7B88CNP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-283-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/23/2024
2	NDC: 79903-283-32	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/23/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	10/23/2024

Labeler - Walmart Inc. (051957769)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(79903-283)