BodyMed 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
BodyMed Alcohol Prep Pad
Generic name
ALCOHOL PREP PAD
Manufacturer
Boxout, LLC
Product type
HUMAN OTC DRUG
SPL set ID
d30dce9c-8d12-4c71-e053-2995a90a1205
SPL ID
4391a16f-7ca3-68ba-e063-6394a90a4250
Version
6
Effective date
2025-11-14
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 05:25:27
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 filre or flame. Do not use in the eyes, on irritated skin, on mucus membrane, and/or with electrocautery procedures.

Reported adverse events (FAERS/openFDA)#

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