FDA.reportPublic FDA data

FDA label 77438aca-55fc-3f9e-e053-2991aa0a3888

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
96916661-9892-4dc1-97ed-b56fc49bcc23
SPL ID
77438aca-55fc-3f9e-e053-2991aa0a3888
Version
3
Effective date
2018-10-02
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:16:15

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 * if solution changes color or become cloudy Ask a doctor if you have * eye pain * changes in vision * redness or irritation of the eye after use * an injury caused by an alkali To avoid contamination, do not touch 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 a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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