FDA.reportPublic FDA data

FDA label 785199ea-3bd6-48ea-afd0-e0c4cf39652b

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
785199ea-3bd6-48ea-afd0-e0c4cf39652b
SPL ID
785199ea-3bd6-48ea-afd0-e0c4cf39652b
Version
1
Effective date
2011-04-20
Source export date
2026-08-01
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/0689a4374f1490600b5244071db3b04bd3bbc29ceda7a856edb8225323adf20a/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:00:29

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 When using this product : ° do not touch tip of container to any surface to avoid contamination ° replace cap after use Stop use and ask a doctor if: ° you experience eye pain, changes in vision, continued redness or irritation of the eye ° condition worsens or persists for more than 72 hours