FDA label 039d7e3c-7d30-4e62-84c9-13c12bce8563

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
81e6bd4b-ff42-4250-a87c-28e2b06d6929
SPL ID
039d7e3c-7d30-4e62-84c9-13c12bce8563
Version
2
Effective date
2018-02-15
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:35:34

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 twist top of single-use container is broken. ● if solution changes color or becomes cloudy. ● 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. ● Do not reuse. Once opened discard. Stop use and ask a doctor i f ● you experience eye pain, changes in vision, continued redness or irritation of the eye. ● 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.

Reported adverse events (FAERS/openFDA)#

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