FDA label 03e127f6-575c-4b15-a59b-2ac1eaecbf9f

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
41dee46f-008d-43b3-b1a6-f161e2d2a2cd
SPL ID
03e127f6-575c-4b15-a59b-2ac1eaecbf9f
Version
2
Effective date
2018-01-09
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:42:31

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 colour or becomes cloudy • for injection • as a contact lens solution. When using the product • do not re-use, once opened, discard. • to avoid contamination, do not touch the tip of the container to any surface. Stop use and consult a doctor if • you experience eye pain. • changes in vision. • continued redness or irritation of the eye. • the condition worsens or persists. Obtain immediate medical treatment for all open wounds in or near the eyes.

Reported adverse events (FAERS/openFDA)#

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