Isopropyl Rubbing Alcohol

Manufacturer
Jell Pharmaceuticals Pvt. Ltd. | Jell Pharmaceuticals Pvt Ltd.
Effective date
2025-11-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:43:21

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 SolutionPSN3
616456isopropyl alcohol 0.5 ML/ML Topical SolutionSCD3
616456isopropyl alcohol 50 % Topical SolutionSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
30400-100-01Isopropyl Rubbing Alcohol355 mL in 1 BOTTLE, PLASTICLIQUID3553
30400-100-02Isopropyl Rubbing Alcohol296 mL in 1 BOTTLE, PLASTICLIQUID2963
30400-100-03Isopropyl Rubbing Alcohol473 mL in 1 BOTTLE, PLASTICLIQUID4733
30400-100-04Isopropyl Rubbing Alcohol946 mL in 1 BOTTLE, PLASTICLIQUID9463
30400-100-05Isopropyl Rubbing Alcohol3785 mL in 1 BOTTLE, PLASTICLIQUID37853
30400-100-06Isopropyl Rubbing Alcohol177 mL in 1 BOTTLE, PLASTICLIQUID1773

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
30400-10030400-100-01, 30400-100-02, 30400-100-03, 30400-100-04, 30400-100-05, 30400-100-06

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-12-17full-release2026-06-01 00:44:58

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 ALCOHOLJell Pharmaceuticals Pvt. Ltd.cd8643ef-dc83-8bc1-e053-2995a90a007b2025-11-11WarningsExact identifier
ndc (package): 30400-100-03
ndc (package): 30400-100-04
ndc (package): 30400-100-05
ndc (package): 30400-100-02
ndc (package): 30400-100-01
ndc (package): 30400-100-06
ndc (product): 30400-100
ndc11 (package): 30400010006
ndc11 (package): 30400010001
ndc11 (package): 30400010003
ndc11 (package): 30400010004
ndc11 (package): 30400010002
ndc11 (package): 30400010005
spl id: 435397e3-f2fa-6fa3-e063-6394a90ad943
spl set id: cd8643ef-dc83-8bc1-e053-2995a90a007b

Reported adverse events (FAERS/openFDA)#

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