Home FDA labels 5ab5b131-0979-42d6-b53b-9117e4d3b4f5 FDA label 5ab5b131-0979-42d6-b53b-9117e4d3b4f5 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 71876336-83de-4baa-a82d-4b056b41bbeb
SPL ID 5ab5b131-0979-42d6-b53b-9117e4d3b4f5
Version 2
Effective date 2019-09-06
Source export date 2026-10-12
Source partition 12
Source file https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:50:24 Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 2 matching rows.
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 When using this product • do not touch tip of container to any surface to avoid contamination Stop use and ask a doctor if • condition worsens or persists for more than 72 hours • you experience eye pain, changes in vision, continued redness or irritation of the eye
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.