FDA label 474d05f7-2c24-caef-e063-6394a90a3a3e

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
df13b0d0-3029-69e1-e053-2a95a90a1759
SPL ID
474d05f7-2c24-caef-e063-6394a90a3a3e
Version
3
Effective date
2025-12-31
Source export date
2026-09-28
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/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:14:54

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 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.