FDA label ee89f6d2-775e-4639-908a-2a6a4674c0d6

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
7faee1af-c126-4786-8e6d-6c07490259fd
SPL ID
ee89f6d2-775e-4639-908a-2a6a4674c0d6
Version
4
Effective date
2017-08-25
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:37:12

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 When using this product • do not touch tip of container to any surface to avoid contamination • replace cap after each use • do not use if solution changes color or becomes cloudy • overuse may cause more eye redness • pupils may become enlarged temporarily • remove contact lenses before using Ask a doctor before use if you have narrow angle glaucoma Stop use and ask a doctor if • you feel eye pain • changes in vision occur • redness or irritation of the eyes lasts • condition worsens or lasts more than 72 hours

Reported adverse events (FAERS/openFDA)#

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