Isopropyl Rubbing Alcohol 70

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 70
Generic name: ISOPROPYL ALCOHOL
Manufacturer: Delon Laboratories (1990) Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: fb481568-0c51-421f-9b73-adb4c84645aa
SPL ID: 54d864c7-cbd9-bab0-e063-6394a90ac2c2
Version: 24
Effective date: 2026-06-22
Source export date: 2026-09-28
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:39:59

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 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Isopropyl Rubbing Alcohol 70	openfda.brand_name
generic name		ISOPROPYL ALCOHOL	openfda.generic_name
manufacturer name		Delon Laboratories (1990) Ltd.	openfda.manufacturer_name
ndc	package	61734-012-10	openfda.package_ndc
ndc	package	61734-012-03	openfda.package_ndc
ndc	package	61734-012-01	openfda.package_ndc
ndc	package	61734-012-06	openfda.package_ndc
ndc	package	61734-012-02	openfda.package_ndc
ndc	package	61734-012-05	openfda.package_ndc
ndc	package	61734-012-09	openfda.package_ndc
ndc	package	61734-012-07	openfda.package_ndc
ndc	package	61734-012-04	openfda.package_ndc
ndc	package	61734-012-08	openfda.package_ndc
ndc	product	61734-012	openfda.product_ndc
ndc11	package	61734001205	derived:openfda.package_ndc
ndc11	package	61734001207	derived:openfda.package_ndc
ndc11	package	61734001209	derived:openfda.package_ndc
ndc11	package	61734001203	derived:openfda.package_ndc
ndc11	package	61734001210	derived:openfda.package_ndc
ndc11	package	61734001208	derived:openfda.package_ndc
ndc11	package	61734001201	derived:openfda.package_ndc
ndc11	package	61734001206	derived:openfda.package_ndc
ndc11	package	61734001204	derived:openfda.package_ndc
ndc11	package	61734001202	derived:openfda.package_ndc
rxcui		808520	openfda.rxcui
spl id		54d864c7-cbd9-bab0-e063-6394a90ac2c2	id
spl set id		fb481568-0c51-421f-9b73-adb4c84645aa	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 if taken internally serious gastric disturbances will result Flammable, keep away from fire or flame 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.