FDA label 45a7fbf2-2d3d-4cb9-9759-4e6cf3f6a96e

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
89c054c5-22c6-40b0-8ef8-8f6e46b56264
SPL ID
45a7fbf2-2d3d-4cb9-9759-4e6cf3f6a96e
Version
4
Effective date
2017-08-25
Source export date
2026-08-08
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-08/e78f1fb32bf83ef6e9a19dc8cb100566f7817d0ac9ed04e609562ab8ed7ab1de/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
b39f3b00ad50d2e1b32aaf429248c6081e8799b35bce715b4fccb8cfa1ac4546
Import run
20260810T161303Z
Imported at
2026-08-10 16:46:54

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 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