FDA.reportPublic FDA data

ISOPROPYL RUBBING ALCOHOL

Manufacturer
KIM CHEMICALS LTD.
Effective date
2009-10-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:54:35

Label at a glance#

ProductISOPROPYL RUBBING ALCOHOL
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Indications and uses

to decrease germs in minor cuts and scrapes. helps relieve minor muscular aches due to exertion.

Dosage and administration

apply to skin directly or with clean gauze, cotton or swab. for rubbing, apply liberally and rub with hands.

Storage and handling

does not contain, nor is intended as a substitute for grain or ethyl alcohol. keep bottle tightly closed.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION


Isopropyl Alcohol  (50% conc.)

Purpose

OTC - PURPOSE SECTION


Topical antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • to decrease germs in minor cuts and scrapes.
  • helps relieve minor muscular aches due to exertion.

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

For external use only

  • flammable, keep away from fire and flame
  • will produce serious gastric disturbances if taken internally

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor before use if you have deep puncture wounds or serious burns

OTC - WHEN USING SECTION

When using this product

  • do not get into eyes or mucous membranes
  • use only in a well-ventilated area

OTC - STOP USE SECTION

Stop use and ask a doctor if condition persists or gets worse.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of an accidental ingestion, contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply to skin directly or with clean gauze, cotton or swab.
  • for rubbing, apply liberally and rub with hands.

Other information

STORAGE AND HANDLING SECTION

  • does not contain, nor is intended as a substitute for grain or ethyl alcohol.
  • keep bottle tightly closed.

Inactive ingredient

INACTIVE INGREDIENT SECTION

purified water

Wintergreen Oil

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
34954-008-122019-10-21C16284748780-1956f9ecf-d10d-621f-e053-dbdaa90a74adPHARMACYS PRESCRIPTION ISOPROPYL ALCOHOL WITH WINTERGREEN OIL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M4163021
ISOPROPYL ALCOHOLACTIVE MOIETYND2M4163021
WATERINACTIVE INGREDIENT059QF0KO0R1

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
34954-00834954-008-12

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
ISOPROPYL ALCOHOLND2M416302ACTIB
WATER059QF0KO0RIACT

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
26eaab39-4dbd-44cb-a17f-1e53f82447f4371fb23e-843c-483d-8694-0e3df2fffa322009-10-01WarningsExact identifier
spl id: 26eaab39-4dbd-44cb-a17f-1e53f82447f4
spl set id: 371fb23e-843c-483d-8694-0e3df2fffa32

Reported adverse events (FAERS/openFDA)#

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