FDA label bf21a686-e306-4dc9-b962-5d313bbc6c9d

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
06b72ff2-2cdb-4a03-8dc1-d2e500c844c1
SPL ID
bf21a686-e306-4dc9-b962-5d313bbc6c9d
Version
4
Effective date
2016-11-02
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:51:10

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 Ask a doctor before use if you have narrow angle glaucoma 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 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 Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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