Equate 876.002/876AC

Manufacturer
Walmart Inc. | Nice-Pak Products, LLC
Effective date
2026-04-29
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:55:14

Label at a glance#

ProductEthyl Alcohol
Active ingredientALCOHOL
Label structure14 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

first aid to help prevent the risk of infection in:

  • minor cuts
  • scrapes
  • burns

Warnings

WARNINGS SECTION

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

Flammable

  • keep away from fire or flame, heat spark, electrical
  • do not use as a fuel source. If exposed to a heat source, vapors may ignite, resulting in severe burns, serious injury, or death.

Ask a doctor before use

OTC - ASK DOCTOR SECTION

for deep or puncture wounds, animal bites or serious burns

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition persists or gets worse

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Caution

PRECAUTIONS SECTION

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

DOSAGE & ADMINISTRATION SECTION

  • 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

INACTIVE INGREDIENT SECTION

acetone, denatonium benzoate, methyl isobutyl ketone, water

Questions or comments?

OTC - QUESTIONS SECTION

1-800-287-1915

Adverse event

ADVERSE REACTIONS SECTION

DSP-TN-21091 DSP-MO-20087

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

Pat. D675,101

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 79903-283-32

equate™

Ethyl Rubbing Alcohol

70% by volume

First Aid Antiseptic

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

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

WARNING FLAMMABLE  

  • keep away from heat, spark, electrical, fire or flame
  • DANGER: DO NOT USE AS A FUEL SOURCE.

If exposed to a heat source, vapors may ignite, resulting in severe burns, serious injury, or death.

Made in the USA with domestic and imported ingredients.

Factory Certified

32 FL OZ (1 QT) 946 mL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN6
582753ethanol 0.7 ML/ML Topical SolutionSCD6
582753ethanol 70 % Topical SolutionSY6
582753ethyl alcohol 70 % Topical SolutionSY6

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData MatrixL0021830BBmm02.jpg
Data codeData MatrixL0021830FBmm01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79903-283-16Ethyl Alcohol473 mL in 1 BOTTLE, PLASTICLIQUID4736
79903-283-32Ethyl Alcohol946 mL in 1 BOTTLE, PLASTICLIQUID9466

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79903-28379903-283-16, 79903-283-32

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52026-02-27monthly-update2026-06-03 17:58:09

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
Ethyl AlcoholETHYL ALCOHOLWalmart Inc.1fd3bed0-8fcc-2cee-e063-6294a90a34fb2026-04-29Warnings, Adverse reactionsExact identifier
ndc (package): 79903-283-16
ndc (package): 79903-283-32
ndc (product): 79903-283
ndc11 (package): 79903028332
ndc11 (package): 79903028316
spl id: 509cff01-9998-f79f-e063-6394a90abdab
spl set id: 1fd3bed0-8fcc-2cee-e063-6294a90a34fb

Reported adverse events (FAERS/openFDA)#

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