FDA label ebacaa05-0ad8-426a-878f-3d01bead2885

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
4a41ba37-556e-4a2e-820a-db9e05ec2a11
SPL ID
ebacaa05-0ad8-426a-878f-3d01bead2885
Version
2
Effective date
2023-03-15
Source export date
2026-09-28
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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:39:24

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. • Remove contact lenses before using • Do not use if this solution changes color or becomes cloudy. • do not touch tip of container to any surface to avoid contamination • replace cap after each use Stop use and ask a doctor if • You feel eye pain, • Changes in vision occur • Redness or irritation of the eye lasts • Condition worsens or lasts more than 72 hours. If pregnant of breast-feeding, ask a health professional before use. Keep out of 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.