ISOPROPYL ALCOHOL

Manufacturer
BROSANT GROUP LLC
Effective date
2023-01-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:53:18

Label at a glance#

ProductISOPROPYL ALCOHOL
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Dosage and administration

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

Storage and handling

-store at room temperature -does not contain, nor is intended as a subsitute for grain or ethyl alcohol

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol (70%conc)

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Warnings

WARNINGS SECTION

For external use only.

-if taken internally, serious gastric disturbances will result

Flammable keep away from fire or flamme

-use only in a well-ventilated area; fumes may be toxic

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 - DO NOT USE 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

condition 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 right away (1-800-222-1222)

Directions

DOSAGE & ADMINISTRATION SECTION

-clean affected area

-apply small amount of this product on the area 1-3 times daily

-if bandaged, let dry first

-may be covered with a sterile bandage

Other information

STORAGE AND HANDLING SECTION

-store at room temperature

-does not contain, nor is intended as a subsitute for grain or ethyl alcohol

Inactive ingredient

INACTIVE INGREDIENT SECTION

purified water

Directions

INDICATIONS & USAGE SECTION

-clean affected area

-apply small amount of this product on the area 1-3 times daily

-if bandaged, let dry first

-may be covered with a sterile bandage

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Isopropyl principal displayIsopropyl principal display

Bioliving

70% isopropyl alcohol

warning flammable

keep away from heat, spark, electrical, fire or flamme

use only in a well-ventilated area; fumes may be harmful

32FL OZ (1QT) 946 mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
808520isopropyl alcohol 70 % Topical SolutionPSN1
808520isopropyl alcohol 0.7 ML/ML Topical SolutionSCD1
808520isopropyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83123-0019-12024-07-30C16284748780-11030e365-6e61-111a-e063-dadaa90a10e2f27d1790-fbc8-5964-e053-2995a90a9898
83123-0019-12024-01-30C16284748780-11030e365-6e61-111a-e063-dadaa90a10e2f27d1790-fbc8-5964-e053-2995a90a9898

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83123-0019-1ISOPROPYL ALCOHOL946 mL in 1 BOTTLELIQUID9461

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83123-0019ISOPROPYL ALCOHOL LIQUID [BROSANT GROUP LLC]11 package rows20230118_f27d1790-fbc8-5964-e053-2995a90a9898.zip

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
83123-001983123-0019-1

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
ISOPROPYL ALCOHOLND2M416302ACTIB
WATER059QF0KO0RIACT

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
f27d1790-fbc9-5964-e053-2995a90a9898f27d1790-fbc8-5964-e053-2995a90a98982023-01-17WarningsExact identifier
spl id: f27d1790-fbc9-5964-e053-2995a90a9898
spl set id: f27d1790-fbc8-5964-e053-2995a90a9898

Reported adverse events (FAERS/openFDA)#

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