Isopropyl Rubbing Alcohol

Manufacturer
New Pride Corp | Jell Pharmaceuticals Pvt. Ltd. | Jell Pharmaceuticals Pvt Ltd.
Effective date
2024-12-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:48:03

Label at a glance#

ProductIsopropyl Rubbing Alcohol
Active ingredientISOPROPYL ALCOHOL
Label structure11 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol (50% conc.)

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

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

SPL UNCLASSIFIED SECTION

  • flammable, keep away from fire or flame, heat, spark, electrical

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep 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 body
  • do not use longer than one week unless directed by a doctor

Stop using this product if

OTC - STOP USE SECTION

  • condition persists or gets worse

Keep this and all drugs out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison control center (1-800-222-1212) immediately

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredient

INACTIVE INGREDIENT SECTION

purified water

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616456isopropyl alcohol 50 % Topical SolutionPSN2
616456isopropyl alcohol 0.5 ML/ML Topical SolutionSCD2
616456isopropyl alcohol 50 % Topical SolutionSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58037-002-01Isopropyl Rubbing Alcohol355 mL in 1 BOTTLE, PLASTICLIQUID3552
58037-002-02Isopropyl Rubbing Alcohol296 mL in 1 BOTTLE, PLASTICLIQUID2962
58037-002-03Isopropyl Rubbing Alcohol473 mL in 1 BOTTLE, PLASTICLIQUID4732
58037-002-04Isopropyl Rubbing Alcohol946 mL in 1 BOTTLE, PLASTICLIQUID9462
58037-002-05Isopropyl Rubbing Alcohol3785 mL in 1 BOTTLE, PLASTICLIQUID37852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58037-002ISOPROPYL RUBBING ALCOHOL (ISOPROPYL ALCOHOL) LIQUID [NEW PRIDE CORP]2Current NDC, Legacy NDC, 5 package rows20241222_f0f12204-2948-1357-e053-2995a90ae50a.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
58037-00258037-002-01, 58037-002-02, 58037-002-03, 58037-002-04, 58037-002-05

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 Rubbing AlcoholISOPROPYL ALCOHOLNew Pride Corpf0f12204-2948-1357-e053-2995a90ae50a2024-12-19WarningsExact identifier
ndc (package): 58037-002-04
ndc (package): 58037-002-01
ndc (package): 58037-002-03
ndc (package): 58037-002-02
ndc (package): 58037-002-05
ndc (product): 58037-002
ndc11 (package): 58037000204
ndc11 (package): 58037000201
ndc11 (package): 58037000203
ndc11 (package): 58037000202
ndc11 (package): 58037000205
spl id: 299ad8d0-051e-1039-e063-6394a90ab780
spl set id: f0f12204-2948-1357-e053-2995a90ae50a

Reported adverse events (FAERS/openFDA)#

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