Alcohol prep pad

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: Alcohol prep pad
Generic name: ALCOHOL PREP PAD
Manufacturer: Target Corporation
Product type: HUMAN OTC DRUG
SPL set ID: bc9a4f33-3eec-79e3-e053-2a95a90a9017
SPL ID: 2e79df47-dc4a-2f9d-e063-6294a90a397f
Version: 4
Effective date: 2025-02-19
Source export date: 2026-10-27
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/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:57:18

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M002	openfda.application_number
brand name		Alcohol prep pad	openfda.brand_name
generic name		ALCOHOL PREP PAD	openfda.generic_name
manufacturer name		Target Corporation	openfda.manufacturer_name
ndc	package	11673-139-01	openfda.package_ndc
ndc	product	11673-139	openfda.product_ndc
ndc11	package	11673013901	derived:openfda.package_ndc
spl id		2e79df47-dc4a-2f9d-e063-6294a90a397f	id
spl set id		bc9a4f33-3eec-79e3-e053-2a95a90a9017	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 heat or flame. Do not use in the eyes or apply over large areas of the body.In case of deep or puncture wounds, animal bites, or serious burns, consulta doctor. Stop use and consulta doctor if the condition persists or gets worse.Do not use longer than 1 week unless directed by a doctor. Keep out of reach of children.If accidentally 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.