FDA label 3415fbca-ad0b-7e3c-e063-6394a90ab53a

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
3415fb52-47c5-0715-e063-6294a90a272c
SPL ID
3415fbca-ad0b-7e3c-e063-6394a90ab53a
Version
1
Effective date
2025-05-01
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:56:59

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.