FDA.reportPublic FDA data

Isopropyl Alcohol

Manufacturer
United Natural Foods, Inc. dba UNFI | Nice-Pak Products, LLC
Effective date
2026-02-26
Label type
HUMAN OTC DRUG LABEL
Version
19
Source
full-release
Hydrated at
2026-06-01 01:47:25

Label at a glance#

ProductIsopropyl Alcohol
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 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 91%

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 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

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

PROVIDENE, RI 02908 USA

855-423-2630

Pat. D675, 101

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 41163-804-45

EQUALINE ®

isopropyl alcohol

first aid antispetic

91% 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 others; 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
582901isopropyl alcohol 91 % Topical SolutionPSN19
582901isopropyl alcohol 0.91 ML/ML Topical SolutionSCD19
582901isopropyl alcohol 91 % Topical SolutionSY19

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41163-804-43Isopropyl Alcohol473 mL in 1 BOTTLE, PLASTICLIQUID47319
41163-804-45Isopropyl Alcohol946 mL in 1 BOTTLE, PLASTICLIQUID94619

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
41163-804-43ML - Milliliter41163-80442093b27-a76b-4398-b806-a8d5992cd4e512016-07-19
41163-804-45ML - Milliliter41163-804baf8fecc-8862-4c19-943f-c284a75b1cb212016-10-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M4163023
ISOPROPYL ALCOHOLACTIVE MOIETYND2M4163023
WATERINACTIVE INGREDIENT059QF0KO0R3

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41163-80441163-804-43, 41163-804-45

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
Isopropyl AlcoholISOPROPYL ALCOHOLUnited Natural Foods, Inc. dba UNFI4eee73dd-039e-44a5-b380-21ff32efee222026-02-26Warnings, Adverse reactionsExact identifier
ndc (package): 41163-804-45
ndc (package): 41163-804-43
ndc (product): 41163-804
ndc11 (package): 41163080443
ndc11 (package): 41163080445
spl id: 4bbbafbc-9110-ab5b-e063-6294a90aedb7
spl set id: 4eee73dd-039e-44a5-b380-21ff32efee22

Reported adverse events (FAERS/openFDA)#

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