Home FDA labels 2517001f-6c1f-8803-e063-6394a90a9593 FDA label 2517001f-6c1f-8803-e063-6394a90a9593 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 563449fc-203a-4446-bfc4-585aa844ecaf
SPL ID 2517001f-6c1f-8803-e063-6394a90a9593
Version 2
Effective date 2024-10-22
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 01:37:34 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 Avoid contact with the eyes. Do not use in large quantities, particularly over raw surfaces or blistered areas. Stop Use and Ask a Doctor if condition worsens or if symptoms persist for more than 7 days or occur again within a few days.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.