Isopropyl Rubbing Alcohol

Manufacturer
7-Eleven, Inc.
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
monthly-update
Hydrated at
2026-06-03 17:51:55

Label at a glance#

ProductIsopropyl Rubbing Alcohol
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Indications and uses

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

Dosage and administration

clean infected area apply 1 to 3 times daily

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Uses

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

SPL UNCLASSIFIED SECTION

  • keep away from fire or flame, heat, spark, electrical. Flash point 72°F
  • do not use with electrocautery procedures.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you havedeep 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 1 week unless directed by a doctor

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • the condition persists or gets worse

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 infected area
  • apply 1 to 3 times daily

Other information

SPL UNCLASSIFIED SECTION

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

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Purified Water

PRINCIPAL DISPLAY PANEL 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rubbing Alcohol

70% Isopropyl

first aid antiseptic

Tamper evident cap for your protection.
If ring-band is detached from cap or missing do not use.

WARNING:Flammable

4 FL. OZ. (118 mL)

PRINCIPAL DISPLAY PANELPRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
808520isopropyl alcohol 70 % Topical SolutionPSN10
808520isopropyl alcohol 0.7 ML/ML Topical SolutionSCD10
808520isopropyl alcohol 70 % Topical SolutionSY10

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130052548512293GTIN-13: 0052548512293
EAN-13: 0052548512293
GTIN-12: 052548512293
UPC-A: 052548512293
GTIN storage (14 digits): 00052548512293
SevenElevenIPA.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10202-002-04Isopropyl Rubbing Alcohol118 mL in 1 BOTTLE, PLASTICSOLUTION11810

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
10202-00210202-002-04

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
92024-11-14full-release2026-06-01 00:37:30

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 ALCOHOL7-Eleven, Inc.96d0488b-decd-4ffc-9179-29905a436bb12026-01-08WarningsExact identifier
ndc (package): 10202-002-04
ndc (product): 10202-002
ndc11 (package): 10202000204
spl id: 47e6563c-d692-3070-e063-6394a90a3d93
spl set id: 96d0488b-decd-4ffc-9179-29905a436bb1

Reported adverse events (FAERS/openFDA)#

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