FDA label 0de2908f-2b9b-414b-9be8-68e26f5a39b6

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
af98b38e-4f2c-431a-a57b-fc03387da51d
SPL ID
0de2908f-2b9b-414b-9be8-68e26f5a39b6
Version
8
Effective date
2018-04-24
Source export date
2026-10-12
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/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:52:23

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 Do not use If solution changes color or becomes cloudy If snap off top is broken or missing When using this product Remove contact lenses before use Do not touch the tip of container to any surface to acoid contamination Stop use and consult a doctor If you experience eye pain, change in vision, continued redness or irritation of the eye If condition worsens or persists If there are open wounds in or near the eye 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.