FDA.reportPublic FDA data

FDA label f4af907f-9ce8-4bb1-961a-61bb157adcf9

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
0ebfbede-6345-4ed4-a817-49e0280d6db1
SPL ID
f4af907f-9ce8-4bb1-961a-61bb157adcf9
Version
4
Effective date
2017-11-02
Source export date
2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:36:06

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: you experience any open wounds in or near the eye and obtain immediate medical treatment. If solution changes color or becomes cloudy. When using this product -To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard Stop use and ask a doctor if you have any of the following: Changes in vision. Eye pain. Condition worsens or persists. Continued redness or irritation of the eye.

Reported adverse events (FAERS/openFDA)#

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