FDA label 9a511d5b-c719-4a2e-81fb-0cc6c55ad8a6

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
f169f613-91b3-47f2-aac1-49cd1d7f6d8a
SPL ID
9a511d5b-c719-4a2e-81fb-0cc6c55ad8a6
Version
2
Effective date
2013-06-19
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 07:29:21

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 • in the eyes or apply over large areas of the body • if you are allergic to any of the ingredients Ask a doctor before use if you have • deep or puncture wounds, animal bites or serious burns Stop use and ask a doctor if • the condition worsen • symptons last more than 7 days or clear up and occur again within a few days

Reported adverse events (FAERS/openFDA)#

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