FDA.reportPublic FDA data

FDA label f42b6382-057f-0e63-e053-2a95a90a211c

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
22e8e404-7ecb-4f2d-bfc7-6ce8d4a333e7
SPL ID
f42b6382-057f-0e63-e053-2a95a90a211c
Version
2
Effective date
2023-02-08
Source export date
2026-09-28
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/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:33

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 • To avoid contamination, do not touch tip of container to any surface • replace cap after using Stop use and ask a doctor if • You experience eye pain • You experience changes in vision • You experience continued redness or irritation of the eye • The condition worsens or persists for more than 72 hours. Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center.

Reported adverse events (FAERS/openFDA)#

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