Home FDA labels eddd9e51-3342-4b2a-873c-5bb647dd98e0 FDA label eddd9e51-3342-4b2a-873c-5bb647dd98e0 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 76e086d8-0e96-4b6b-b9bc-c7b98a02e300
SPL ID eddd9e51-3342-4b2a-873c-5bb647dd98e0
Version 3
Effective date 2024-11-25
Source export date 2026-10-12
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:03:51 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 For external use only Do not use on open cuts When using this product do not get into eyes Do not ingest Stop use and ask a doctor if: Condition worsens Sensitivity develops or increases Symptoms last more than 7 days or clear up and occur again in a few days
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.