FDA label 67927feb-5dd8-4113-b4fa-5a991a4c901b

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
f382e069-5c06-4fd2-ba34-2d187366f8f9
SPL ID
67927feb-5dd8-4113-b4fa-5a991a4c901b
Version
3
Effective date
2024-11-14
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:08:48

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 • pupils may become enlarged temporarily • overuse may cause more redness of the eye • remove contact lenses before using • replace cap after each use • do not use if solution changes color or becomes cloudy • do not touch tip of container to any surface to avoid contamination Stop use and ask a doctor if • you feel eye pain • changes in vision occur • redness or irritation of the eye lasts • condition worsens or persists for more than 72 hours Keep Out of Reach of Children If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Reported adverse events (FAERS/openFDA)#

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