FDA label 4298c46d-2fc3-44f2-b096-fbce32d993fa

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
034d4d69-39e1-4492-9033-9a744bafbe0c
SPL ID
4298c46d-2fc3-44f2-b096-fbce32d993fa
Version
1
Effective date
2012-08-27
Source export date
2026-09-28
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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:41:12

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. Obtain immediate medical treatment for all open wounds in or near the eye To avoid contamination, do not touch tip of container to any surface Do not reuse Discard vial after use Do not use if: Solution changes color or becomes cloudy With contact lenses If vial is open or seal is broken. Stop use and consult a doctor if you experience: Eye pain Changes in vision Continued redness or irritation of the eye or if the condition worsens or persists. 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.