Home FDA labels 18a909f2-c5d1-2c42-e054-00144ff88e88 FDA label 18a909f2-c5d1-2c42-e054-00144ff88e88 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 18a909f2-c5d0-2c42-e054-00144ff88e88
SPL ID 18a909f2-c5d1-2c42-e054-00144ff88e88
Version 1
Effective date 2015-06-16
Source export date 2026-11-06
Source partition 13
Source file https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/245ea1c0d730b312e4410f082201cbe2cb4d1936fa2918316b6ea631293cbeba/drug-label-0013-of-0014.json.zip
Source manifest SHA-256 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run 20261108T063105Z
Imported at 2026-11-08 08:06:11 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 FOR EXTERNAL USE ONLY WHEN USING THIS PRODUCT Avoid contact with eyes. if contact occurs, rinse eyes thoroughly with water. STOP USE AND ASK A DOCTOR IF condition worsens or does not improve after regular use of this procuct as directed.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.