Isopropyl Rubbing Alcohol 70%

Manufacturer
AgroChem, Inc | Aimee Trader | AgoChem, Inc
Effective date
2020-09-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:33:27

Label at a glance#

ProductIsopropyl Rubbing Alcohol 70%
Active ingredientISOPROPYL ALCOHOL
Label structure13 sections

Dosage and administration

Clean the affected area. Apply a small amount of this product 1 to 3 times daily May be covered with a sterile bandage. If bandaged, let dry first..

Storage and handling

Store at room temperature ∙ does not contain nor intended as a substitute for grain or ethyl alcohol ∙ will produce serious gastric disturbances if taken internally.

Label contents#

Full prescribing information#

DESCRIPTION SECTION

Isopropyl Rubbing Alcohol 70%

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70% v/v Purpose:First Aid Antiseptic

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Use

INDICATIONS & USAGE SECTION

First aid to help prevent the risk of infection in: ∙ minor cuts ∙ scrapes ∙ burns.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame, heat spark, electrical, Flash point 72F ∙ do not use with electrocautery procedures.

Do not use

OTC - DO NOT USE SECTION

When using this product ∙ do not use in or near the eyes ∙ do not apply to large areas of the body ∙ do not use longer than 1 week unless directed by a doctor

OTC - WHEN USING SECTION

Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns.

OTC - STOP USE SECTION

Ask a doctor before use if the condition persists or gets worse

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion seek professional assistance or contact Poison Control Center (1-800-222-1222)

Directions

DOSAGE & ADMINISTRATION SECTION

Clean the affected area. Apply a small amount of this product 1 to 3 times daily May be covered with a sterile bandage.

If bandaged, let dry first..

Other information

STORAGE AND HANDLING SECTION

Store at room temperature ∙ does not contain nor intended as a substitute for grain or ethyl alcohol ∙ will produce serious gastric disturbances if taken internally.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4 oz label4 oz label118 mL NDC: 17307-1201-1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
808520isopropyl alcohol 70 % Topical SolutionPSN2
808520isopropyl alcohol 0.7 ML/ML Topical SolutionSCD2
808520isopropyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17307-1201-12022-01-28C16284748780-1d6a99b39-4ac8-a426-e053-dadaa90af4c2Isopropyl Rubbing Alcohol 70%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17307-1201-1Isopropyl Rubbing Alcohol 70%118 mL in 1 BOTTLE, SPRAYSOLUTION1182

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17307-1201ISOPROPYL RUBBING ALCOHOL 70% (ALCOHOL) SOLUTION [AGROCHEM, INC]2Legacy NDC, 1 package rows20201113_a7a6e6f7-5485-3366-e053-2995a90ad486.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17307-120117307-1201-1

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
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
afd81601-666f-680e-e053-2a95a90a858da7a6e6f7-5485-3366-e053-2995a90ad4862020-09-21WarningsExact identifier
spl id: afd81601-666f-680e-e053-2a95a90a858d
spl set id: a7a6e6f7-5485-3366-e053-2995a90ad486

Reported adverse events (FAERS/openFDA)#

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