FDA label d82436ff-6bb2-aaff-e053-2995a90abe02

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
55f3133c-da81-46f2-998a-8364def05ff8
SPL ID
d82436ff-6bb2-aaff-e053-2995a90abe02
Version
3
Effective date
2022-02-16
Source export date
2026-11-06
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/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:31:01

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 Do not use : • On deep or puncture wound • Animal bites • Serious burns • If skin allergy problem occurs When using this product : Avoid contact with eyes or mouth, avoid eat seafood or hot food Stop use and ask a doctor if : • Condition Worsens • Symptom clear up and occur again within a few days • Symptom persist for more than 7 days

Reported adverse events (FAERS/openFDA)#

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