FDA label f42b5aca-6d82-2a78-e053-2a95a90a342a

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
cad56a48-05fe-449a-af63-519f073a1533
SPL ID
f42b5aca-6d82-2a78-e053-2a95a90a342a
Version
2
Effective date
2023-02-08
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:23:37

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 product if solution changes color or becomes cloudy. Stop use and ask a doctor if you experience • Eye pain, • Changes in vision, • Continued redness or irritation of the eye or if the condition worsens or persists for more than 72 hours. When using this product: • To avoid contamination, do not touch tip of container to any surface. • Replace cap after using. Keep container tightly closed. • Remove contact lens before using Keep out of reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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