FDA.reportPublic FDA data

FDA label 3cde6734-8bf5-66e2-e054-00144ff8d46c

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
bd80d24d-fa37-4766-bf92-90382fdee58a
SPL ID
3cde6734-8bf5-66e2-e054-00144ff8d46c
Version
1
Effective date
2016-09-19
Source export date
2026-11-06
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/5731a8c92e1c0dd2a09d2f92b410e7a70ea29cbf6b8040a6a05e4be5b7c51f0d/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:41:58

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 for injection in intraocular surgery internally internally if solution changes color or becomes cloudy Ask a doctor if you have eye pain cahnges in vision redness or irritation of the eye after use an injury caused by an alkili To avoid contamination, do not touch the tip of container to any surface. Do not reuse. Once opened, discard. Keep out of reach of children. If swallowed, get medical help or contact Poison control Center right away.

Reported adverse events (FAERS/openFDA)#

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