FDA label 977450fc-14a0-4bad-b5a5-af98ae25ab06

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
9b6b900e-39c1-4746-a7e7-cb79b6339fcb
SPL ID
977450fc-14a0-4bad-b5a5-af98ae25ab06
Version
7
Effective date
2023-02-21
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:36:44

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 • if solution changes color or becomes cloudy When using this product • do not touch tip of container to any surface to avoid contamination • remove contact lenses before using • replace cap after using Stop use and ask a doctor if you experience • eye pain • changes in vision • continued redness or irritation of the eye • or if condition worsens or lasts more than 72 hours If pregnant or breastfeeding , ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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