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
2026-09-28
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 05:24:54
Harmonized routes table
Harmonized routes
TOPICAL

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.