FDA label d81d474e-414e-4646-9ff1-663ffb84267a

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
92a58e9b-e420-4e4c-aec8-c9a068d67347
SPL ID
d81d474e-414e-4646-9ff1-663ffb84267a
Version
1
Effective date
2024-03-08
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:38:41

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 this product changes color or becomes cloudy Ask a doctor before using if you have narrow angle glaucoma When using this product replace cap after each use overuse may cause more redness of the eye pupils may become enlarged temporarily to avoid contamination do not touch tip of container to any surface Stop use and ask a doctor if you experience eye pain experience changes in vision experience continued redness or irritation of the eye the condition worsens or symptoms last for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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