Non-proprietary name

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
Non-proprietary name
Generic name
ALCOHOL PREP PAD
Manufacturer
Guangzhou Four E's Scientific Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
edb4a43a-5b55-3404-e053-2a95a90ada27
SPL ID
3c9d0749-4ed4-e619-e063-6394a90af263
Version
6
Effective date
2025-08-18
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 05:34:00
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 fire or flame - Do not use with electrocautery procedures - Do not use in the eyes - Do not apply to irritated skin - Stop use if pain, irritation, redness, or swelling occurs, discontinue use and consult a physician Keep out of reach of children

Reported adverse events (FAERS/openFDA)#

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