FDA label ffb8fd28-735b-47f1-87fe-fa9214c72423

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
84d70d2c-9c2e-4139-8d1c-c2f3ccbd2cab
SPL ID
ffb8fd28-735b-47f1-87fe-fa9214c72423
Version
2
Effective date
2017-07-14
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:30:00

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 Warnings: DO NOT USE IF YOU ARE OVER SENSITIVE OR ALLERGIC TO THIS PRODUCT. DO NOT USE IF YOU HAVE ANY DISORDER OR OPEN WOUND AROUND THE EYE. KEEP OUT OF REACH OF CHILDREN. KEEP CAP FIRMLY CLOSED WHEN NOT IN USE. STORE IN A COOL. DARK PLACE AND AVOID DIRECT SUNLIGHT. AVOID DIRECT CONTACT WITH THE EYES AND MUCOUS MEMBRANES.

Reported adverse events (FAERS/openFDA)#

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