Isopropyl Rubbing Alcohol

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Isopropyl Rubbing Alcohol
Generic name: ISOPROPYL ALCOHOL
Manufacturer: NDC, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 07bfadf4-7452-4c7a-b60e-feb658b92e73
SPL ID: 47e5c09a-4f6a-9963-e063-6394a90a3476
Version: 12
Effective date: 2026-01-08
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:20:22

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Isopropyl Rubbing Alcohol	openfda.brand_name
generic name		ISOPROPYL ALCOHOL	openfda.generic_name
manufacturer name		NDC, Inc.	openfda.manufacturer_name
ndc	package	43128-002-16	openfda.package_ndc
ndc	package	43128-002-32	openfda.package_ndc
ndc	package	43128-002-01	openfda.package_ndc
ndc	product	43128-002	openfda.product_ndc
ndc11	package	43128000201	derived:openfda.package_ndc
ndc11	package	43128000232	derived:openfda.package_ndc
ndc11	package	43128000216	derived:openfda.package_ndc
rxcui		808520	openfda.rxcui
spl id		47e5c09a-4f6a-9963-e063-6394a90a3476	id
spl set id		07bfadf4-7452-4c7a-b60e-feb658b92e73	set_id
unii		ND2M416302	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS For external use only Flammable keep away from fire or flame, heat, spark, electrical. Flash point 72°F do not use with electrocautery procedures. Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns. When using this product 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 the condition persists or gets worse Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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