FDA.reportPublic FDA data

FDA label f42ac0ee-2d86-1dfb-e053-2995a90aa656

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
ec7944f0-3a46-45c7-81d1-1d828e857456
SPL ID
f42ac0ee-2d86-1dfb-e053-2995a90aa656
Version
2
Effective date
2023-02-08
Source export date
2026-10-12
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/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:05:53

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 Do not use except under the advice and supervision of a doctor When using this product • It may cause temporary burning and irritation • Replace cap after use • To avoid contamination do not touch tip of container to any surface. Stop use and ask a doctor if • Condition worsens or persists for more than 72 hours. • You experience eye pain, changes in vision, continued redness or irritation of the eye Keep out of the 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.