FDA label 48e0a769-7c15-445f-b36a-a2fa2630f900

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
d5eb1bb1-0922-45ce-842c-ee0b33704f06
SPL ID
48e0a769-7c15-445f-b36a-a2fa2630f900
Version
3
Effective date
2019-02-06
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:49:44

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 Ask a doctor before use if you have narrow angle glaucoma When using this product ▪ pupils may become enlarged temporarily ▪ overuse may produce increased redness of the eye ▪ remove contact lenses before using ▪ to avoid contamination, do not touch tip of container to any surface ▪ replace cap after using Stop use and ask a doctor if ▪ you experience eye pain ▪ you experience changes in vision ▪ you experience 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 (1-800-222-1222) center right away.

Reported adverse events (FAERS/openFDA)#

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