FDA.reportPublic FDA data

70%

Manufacturer
United Natural Foods, Inc. dba UNFI | Nice-Pak Products, LLC
Effective date
2026-02-26
Label type
HUMAN OTC DRUG LABEL
Version
18
Source
full-release
Hydrated at
2026-06-01 01:47:26

Label at a glance#

Product70%
Active ingredientISOPROPYL ALCOHOL
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 affected 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

Isopropyl 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

WARNINGS AND 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 affected area 1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first

Other information

OTHER SAFETY INFORMATION

  • does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive ingredient

INACTIVE INGREDIENT SECTION

water

ADVERSE REACTION

ADVERSE REACTIONS SECTION

Distributed by UNFI

Providence, RI 02908 USA

855-423-2360

Pat. D675, 101

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 41163-073-45

EQUALINE ®

isopropyl rubbing alcohol

first aid antiseptic

70% isopropyl alcohol by volume

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.

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

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

32 FL OZ (1 QT) 946 mL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
808520isopropyl alcohol 70 % Topical SolutionPSN18
808520isopropyl alcohol 0.7 ML/ML Topical SolutionSCD18
808520isopropyl alcohol 70 % Topical SolutionSY18

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41163-073-4370%473 mL in 1 BOTTLE, PLASTICLIQUID47318
41163-073-4570%946 mL in 1 BOTTLE, PLASTICLIQUID94618
41163-073-7270%296 mL in 1 BOTTLE, SPRAYLIQUID29618

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
41163-073-43ML - Milliliter41163-073275fe901-40e5-4fae-89fc-a63833e87e6112017-03-06
41163-073-45ML - Milliliter41163-07332a6818d-405c-4003-acc4-530e152942cf12016-10-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M4163021
ISOPROPYL ALCOHOLACTIVE MOIETYND2M4163021
waterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41163-07341163-073-43, 41163-073-45, 41163-073-72

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
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
70%ISOPROPYL ALCOHOLUnited Natural Foods, Inc. dba UNFId39bc652-442d-4d91-9eba-a496636b95332026-02-26Warnings, Adverse reactionsExact identifier
ndc (package): 41163-073-72
ndc (package): 41163-073-45
ndc (package): 41163-073-43
ndc (product): 41163-073
ndc11 (package): 41163007345
ndc11 (package): 41163007372
ndc11 (package): 41163007343
spl id: 4bbbd9b1-cd40-e4d1-e063-6394a90aac2a
spl set id: d39bc652-442d-4d91-9eba-a496636b9533

Reported adverse events (FAERS/openFDA)#

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