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
2026-11-06
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/2026-11-06/10387d7618367cd955339e75d48af3d11f99f789153db05c529d9fad6eccc645/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:19:36

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.