Curad Alcohol Prep Pads 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: Curad Alcohol Prep Pads Medium
Generic name: ISOPROPYL ALCOHOL
Manufacturer: Medline Industries, LP
Product type: HUMAN OTC DRUG
SPL set ID: 1ce3872e-2307-4a38-bd7d-7eb2b226cf3c
SPL ID: 5aae9c64-86d9-8202-e063-6294a90a551b
Version: 20
Effective date: 2026-09-04
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:52

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Curad Alcohol Prep Pads Medium	openfda.brand_name
generic name		ISOPROPYL ALCOHOL	openfda.generic_name
manufacturer name		Medline Industries, LP	openfda.manufacturer_name
ndc	package	53329-827-09	openfda.package_ndc
ndc	package	53329-827-29	openfda.package_ndc
ndc	package	53329-827-60	openfda.package_ndc
ndc	package	53329-827-30	openfda.package_ndc
ndc	package	53329-827-33	openfda.package_ndc
ndc	package	53329-827-36	openfda.package_ndc
ndc	package	53329-827-40	openfda.package_ndc
ndc	product	53329-827	openfda.product_ndc
ndc11	package	53329082736	derived:openfda.package_ndc
ndc11	package	53329082729	derived:openfda.package_ndc
ndc11	package	53329082730	derived:openfda.package_ndc
ndc11	package	53329082760	derived:openfda.package_ndc
ndc11	package	53329082709	derived:openfda.package_ndc
ndc11	package	53329082740	derived:openfda.package_ndc
ndc11	package	53329082733	derived:openfda.package_ndc
rxcui		797544	openfda.rxcui
spl id		5aae9c64-86d9-8202-e063-6294a90a551b	id
spl set id		1ce3872e-2307-4a38-bd7d-7eb2b226cf3c	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. Do not use with electrocautery procedures longer than 1 week unless directed by a physician When using this product do not get into eyes do not apply over large areas of the body in case of deep or puncture wounds, animal bites or serious burns, consult a doctor Stop use and ask a doctor if irritation and redness develop condition gets worse or persists for more than 72 hours Keep out of reach of children. If accidentally swallowed, seek medical assistance or immediately contact a Poison Control Center.

Reported adverse events (FAERS/openFDA)#

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