FDA label 21e393f3-2ada-4fb8-845b-95bc6ff565cc

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
b990b342-4f37-4782-b066-cf6ad696c92a
SPL ID
21e393f3-2ada-4fb8-845b-95bc6ff565cc
Version
2
Effective date
2011-04-04
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:22:48

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. Overuse of this product may produce increased redness of the eye. When using this product pupils may become enlarged temporarily. Ask a doctor before use if you have narrow angle glaucoma. Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours. To avoid contamination, do not touch tip of container to any surface. Replace cap after using. Do not use if solution changes color or becomes cloudy. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Directions Instill 1 or 2 drops in the affected eye(s) up to four times daily.

Reported adverse events (FAERS/openFDA)#

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