Medline Alcohol Prep Sterile, Medium

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: Medline Alcohol Prep Sterile, Medium
Generic name: ISOPROPYL ALCOHOL
Manufacturer: Medline Industries, LP
Product type: HUMAN OTC DRUG
SPL set ID: 9a8584e1-b422-4b77-8464-4e022d578fad
SPL ID: 41489446-e231-53ab-e063-6394a90a9ed0
Version: 20
Effective date: 2025-10-16
Source export date: 2026-09-28
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:34:15

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Medline Alcohol Prep Sterile, Medium	openfda.brand_name
generic name		ISOPROPYL ALCOHOL	openfda.generic_name
manufacturer name		Medline Industries, LP	openfda.manufacturer_name
ndc	package	53329-805-09	openfda.package_ndc
ndc	package	53329-805-86	openfda.package_ndc
ndc	package	53329-805-30	openfda.package_ndc
ndc	package	53329-805-57	openfda.package_ndc
ndc	package	53329-805-97	openfda.package_ndc
ndc	package	53329-805-60	openfda.package_ndc
ndc	product	53329-805	openfda.product_ndc
ndc11	package	53329080530	derived:openfda.package_ndc
ndc11	package	53329080597	derived:openfda.package_ndc
ndc11	package	53329080586	derived:openfda.package_ndc
ndc11	package	53329080509	derived:openfda.package_ndc
ndc11	package	53329080560	derived:openfda.package_ndc
ndc11	package	53329080557	derived:openfda.package_ndc
rxcui		797544	openfda.rxcui
spl id		41489446-e231-53ab-e063-6394a90a9ed0	id
spl set id		9a8584e1-b422-4b77-8464-4e022d578fad	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. When using this product do not get in the eyes or apply over large areas of the body in case of deep or puncture wounds, animal bites or serious burns, consult a doctor 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.