FDA.reportPublic FDA data

FDA label c1da5f7a-a1aa-4bdc-aae7-03d3ab82dc50

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
f77ff717-ccb4-4e0c-a6e6-023f62fac02c
SPL ID
c1da5f7a-a1aa-4bdc-aae7-03d3ab82dc50
Version
2
Effective date
2013-07-09
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:50:07

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 Ask a doctor if you have narrow angle glaucoma When using this product • do not touch tip of container to any surface to avoid contamination • replace cap after each use • do not use if solution changes color or becomes cloudy • overuse may cause eye redness • pupils may become enlarged temporarily • remove contact lenses before using Stop use and ask a doctor if • you feel eye pain • changes in vision occur • redness or irritation of the eyes lasts • condition worsens or lasts more than 72 hours

Reported adverse events (FAERS/openFDA)#

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