FDA.reportPublic FDA data

FDA label 9d13ab3b-bf0d-4b35-b7a5-4c97dc073365

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
c0549236-9a46-3306-e053-2995a90a2011
SPL ID
9d13ab3b-bf0d-4b35-b7a5-4c97dc073365
Version
2
Effective date
2024-11-20
Source export date
2026-11-06
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/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:02:28

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 this product • if solution changes color or becomes cloudy When Using this product • remove contact lens before using • to avoid contamination, do not touch tip of container to any surface • replace cap after using. Keep container tightly closed. Stop Use and ask a doctor if you experience • eye pain • changes in vision • continued redness or irritation of the eye or if the condition worsens or persists for more than 72 hours

Reported adverse events (FAERS/openFDA)#

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