Isopropyl Alcohol 91%

Manufacturer
Virgin Scent Inc.
Effective date
2022-07-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:50:15

Label at a glance#

ProductIsopropyl Alcohol 91%
Active ingredientISOPROPYL ALCOHOL
Label structure8 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredients (by volume)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol, 91%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Use[s]

INDICATIONS & USAGE SECTION

first aid to help prevent the risk of infection in minor cuts, scrapes, and burns.

Warnings

WARNINGS SECTION

For external use only. Flammable.

  • Keep away from fire, flame, heat, spark, electricity.
  • If taken internally, serious gastric disturbances will result.
  • Use only in 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 - WHEN USING SECTION

  • do not get into eyes.
  • do not apply over large areas of the body.
  • do not use longer than week unless directed by a doctor.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition persists or gets worse
  • do not use other-wise than directed

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 (1-800-222-1222) immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-855-238-4488

Packag Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582901isopropyl alcohol 91 % Topical SolutionPSN2
582901isopropyl alcohol 0.91 ML/ML Topical SolutionSCD2
582901isopropyl alcohol 91 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78706-002-162024-01-30C16284748780-11030e365-5d31-111a-e063-dadaa90a10e2Isopropyl Alcohol 91%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78706-002-16Isopropyl Alcohol 91%473 mL in 1 BOTTLELIQUID4732

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78706-002ISOPROPYL ALCOHOL 91% (ISOPROPYL ALCOHOL) LIQUID [VIRGIN SCENT INC.]2Legacy NDC, 1 package rows20220722_ae406480-406c-1a70-e053-2a95a90afb6d.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
78706-00278706-002-16

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
e4569f5d-b1d4-bd78-e053-2a95a90a7c52ae406480-406c-1a70-e053-2a95a90afb6d2022-07-21WarningsExact identifier
spl id: e4569f5d-b1d4-bd78-e053-2a95a90a7c52
spl set id: ae406480-406c-1a70-e053-2a95a90afb6d

Reported adverse events (FAERS/openFDA)#

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