FDA label f1a500e0-ee72-4dc5-b8c4-dbc55799ff32

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)

SPL set ID
e27aaebb-2fab-4e18-b745-b87722ab7182
SPL ID
f1a500e0-ee72-4dc5-b8c4-dbc55799ff32
Version
1
Effective date
2020-04-24
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:47:41

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, heat, spark, electrical Ask a doctor before use if you have • deep punctured wounds, animal bites or serious burns Whe using this product • do not get into eyes • do not apply over large areas of the body • do not use longer than one week unless directed by a doctor Stop using this product if • condition persists or gets worse Keep this and all drugs out of the reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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