FDA label 10ccbeaf-d9ee-498b-acc5-380982ea11a7

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
cb73a3bb-40fc-4535-a575-6c0886d20b70
SPL ID
10ccbeaf-d9ee-498b-acc5-380982ea11a7
Version
3
Effective date
2016-10-03
Source export date
2026-10-12
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:49:51

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 before use 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 more 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.