FDA label 5c6ba700-0a7f-4231-abfa-f0726955579a

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
662e1fff-47be-488d-be48-4dc6df1efd19
SPL ID
5c6ba700-0a7f-4231-abfa-f0726955579a
Version
1
Effective date
2018-01-19
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:34:11

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 solution changes color. ● if you are sensitive to any ingredient in this product. When using this product ● avoid contamination, do not touch tip of container to any surface. ● replace cap after each use. ● remove contact lenses. Stop use and ask a doctor i f ● you experience eye pain, changes in vision, continued redness or irritation of the eye(s). ● the condition worsens or persists 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 (1-800-222-1222).

Reported adverse events (FAERS/openFDA)#

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