FDA label d38a90ce-4733-4abb-a2ac-8176273a6515

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
d38a90ce-4733-4abb-a2ac-8176273a6515
SPL ID
d38a90ce-4733-4abb-a2ac-8176273a6515
Version
1
Effective date
2014-07-15
Source export date
2026-10-12
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:26:26

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 solution changes color or becomes cloudy When using this product • Remove contact lenses before using • Avoid contamination, do not touch tip of container to any surface • Do not reuse, once open, discard Stop use and ask a doctor if • You experience eye pain • Changes in vision occur • Continued redness or irritation of the eye or if the condition worsens or persists • Obtain immediate medical treatment for all open wounds in or near the eyes 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.