FDA label f22b9522-ce4f-4da3-8345-21e9b43ca265

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
a34c8c42-2b17-49db-ae24-acab22515282
SPL ID
f22b9522-ce4f-4da3-8345-21e9b43ca265
Version
2
Effective date
2013-08-20
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:32:38

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings

FOR EXTERNAL USE ONLY. DO NOT USE IN THE EYES.

warnings table

<table border="0" cellpadding="0" cellspacing="0" width="632" ID="i3024761c-63b8-4086-8e91-17a693fbc893"> <col width="632"/> <tbody> <tr> <td>FOR EXTERNAL USE ONLY.<content> </content> </td> </tr> <tr> <td>DO NOT USE IN THE EYES.</td> </tr> </tbody> </table>

Reported adverse events (FAERS/openFDA)#

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