FDA.reportPublic FDA data

91% Isopropyl Alcohol

Manufacturer
Streamline Polymers LLC
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:46:49

Label at a glance#

Product91% Isopropyl Alcohol
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Dosage and administration

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

Storage and handling

does not contain, nor is intended as a substitute for grain or ethyl alcohol will produce serious gastric disturbances if taken internally

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This is a first aid antiseptic. It is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients:

  1. Isopropyl Alcohol (91%, v/v) in an aqueous solution.
  2. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 91% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

helps prevent the risk of infection in minor cuts, scrapes, burns.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame, heat, spark, electrical

OTC - WHEN USING SECTION

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.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

  • does not contain, nor is intended as a substitute for grain or ethyl alcohol
  • will produce serious gastric disturbances if taken internally

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

16 oz 91% NDC: 74793-0009-216 oz 91% NDC: 74793-0009-2946 mL NDC: 74793-0009-1946 mL NDC: 74793-0009-1946 ml NDC: 74793-0009-1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582901isopropyl alcohol 91 % Topical SolutionPSN3
582901isopropyl alcohol 0.91 ML/ML Topical SolutionSCD3
582901isopropyl alcohol 91 % Topical SolutionSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74793-0009-12023-07-28C16284748780-10191ceaa-6aa5-198a-e063-dbdaa90aec3e91% Isopropyl Alcohol Antiseptic

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74793-0009-191% Isopropyl Alcohol946 mL in 1 BOTTLELIQUID9463

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74793-000991% ISOPROPYL ALCOHOL LIQUID [STREAMLINE POLYMERS LLC]3Legacy NDC, 1 package rows20220114_af613ab6-174e-6dc4-e053-2a95a90af606.zip

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
74793-000974793-0009-1

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
d57b2b5a-3d5d-1e2e-e053-2995a90afca1af613ab6-174e-6dc4-e053-2a95a90af6062022-01-13WarningsExact identifier
spl id: d57b2b5a-3d5d-1e2e-e053-2995a90afca1
spl set id: af613ab6-174e-6dc4-e053-2a95a90af606

Reported adverse events (FAERS/openFDA)#

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