FDA label b96792af-b672-4629-93f8-0575106501fe

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
306de2bf-4d5b-4421-8049-fdcfe9fd10eb
SPL ID
b96792af-b672-4629-93f8-0575106501fe
Version
2
Effective date
2018-04-18
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:52:13

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 use in the eye s only . Retain outer carton for full product drug facts. Do not use if this product changes color or becomes cloudy. if you are sensitive to any ingredient in this product. When using this product do not touch tip of container to any surface avoid contamination. remove contact lenses replace cap after each use. do not deliver more than 6 consecutive drops. Stop use and ask a doctor if you feel eye pain. changes in vision occur. redness or irritation of the eye(s) gets worse, persists or lasts more than 72 hours. Keep this and all drugs 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.