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
2026-11-06
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/2026-11-06/bbdc0a42bf44145a63c3752991067bece7e2a518be6cc14943d33c4987faa012/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:09:50

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.