FDA label 288a1f32-8469-3958-e063-6394a90ae41a

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
f4ea9ae8-c783-48b4-af31-a26ecaa34992
SPL ID
288a1f32-8469-3958-e063-6394a90ae41a
Version
7
Effective date
2024-12-05
Source export date
2026-11-06
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/2026-11-06/10387d7618367cd955339e75d48af3d11f99f789153db05c529d9fad6eccc645/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:16:01

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. Avoid contact with eyes. In case of contact, flush thoroughly with water. Ask a doctor before use if you have , deep of puncture wounds, animal bites, serious burns When using this product, do not apply to areas of raw or blistered skin in large quantities, do not use in or near the eyes Stop use and ask a doctor if , condition worsens, symptoms last for more than 7 days or clear up and recur within a few days

Reported adverse events (FAERS/openFDA)#

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