FDA label bf8f89d0-0c43-542f-e053-2995a90a3dee

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
e6b73558-ea08-44b1-a616-421d9f8423e3
SPL ID
bf8f89d0-0c43-542f-e053-2995a90a3dee
Version
1
Effective date
2021-04-09
Source export date
2026-09-28
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/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:29:07

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 You are sensitive to any ingredient in this product Tab on vial is torn, broken, or missing When using this product Do not touch tip of container to any surface to avoid contamination Do not reuse Once opened, discard Stop use and ask a doctor if You experience eye pain You experience changes in vision You experience continued redness or irritation Condition worsens Symptoms last more than 72 hors 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.