FDA label 474cf113-4ac8-f14a-e063-6294a90a3c79

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
df0236d2-e65a-0896-e053-2995a90a7a8d
SPL ID
474cf113-4ac8-f14a-e063-6294a90a3c79
Version
3
Effective date
2025-12-31
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:27:42

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 use in the eye only Do not use if you use a monoamine oxidase inhibitor (MAOI) if solution changes colour or becomes cloudy. Ask a doctor or pharmacist before use if you have narrow angle glaucoma are pregnant or breastfeeding. When using this product pupils may become enlarged temporarily to avoid contamination, do not touch tip of the container to any surface replace cap after using overuse of this product may cause increased redness of the eye. Stop use and ask a doctor if you have a headache, eye pain, changes in vision, redness or irritation of the eye symptoms worsen or last longer than 3 days. Keep out of the reach of children. If swallowed, call a poison control centre or get medical help right away.

Reported adverse events (FAERS/openFDA)#

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