FDA label 4e60a582-a182-4e99-e063-6294a90a43cf

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
e3d60c20-7cbc-4728-8e42-441b64608b88
SPL ID
4e60a582-a182-4e99-e063-6294a90a43cf
Version
6
Effective date
2026-04-01
Source export date
2026-08-01
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/29baabee7fa6726d72190670d84f1571113181a958a8119cbe97e8f0d1d955b2/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:14:50

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 Do not use ■ if solution changes color or becomes cloudy A sk a doctor before use if you have ■ narrow angle glaucoma When using this product ■ to avoid contamination, do not touch tip of container to any surface ■ replace cap after using ■ overuse of this product may produce increased redness of the eye ■ pupils may become enlarged temporarily Stop use and ask a doctor if ■ you experience: ■ eye pain ■ changes in vision ■ continued redness or irritation of the eye ■ 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.