FDA label 33e35e81-4aa7-1538-e063-6394a90a9c7c

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
327b4168-7242-df4d-e063-6394a90ab6a6
SPL ID
33e35e81-4aa7-1538-e063-6394a90a9c7c
Version
2
Effective date
2025-04-28
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:32:09

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

For external use only Do not use on deep or puncture wounds, animal bites, or serious burns unless directed by a doctor Discontinue use and consult a dermatologist if any of the following symptoms occur, as continued use may worsen the condition: 1) Red spots, swelling, itching, or irritation during use; 2) Similar symptoms appearing on the applied area due to direct sunlight exposure Avoid contact with eyes; if contact occurs, rinse immediately Keep out of reach of children Store in a cool, dry place, away from direct sunlight and extreme temperatures

Reported adverse events (FAERS/openFDA)#

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