Home FDA labels 6f56256b-561e-438d-8eb3-35b7d14da253 FDA label 6f56256b-561e-438d-8eb3-35b7d14da253 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 fe73a0e5-9fac-4d8e-9e2e-081bf85348ac
SPL ID 6f56256b-561e-438d-8eb3-35b7d14da253
Version 3
Effective date 2010-05-25
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 08:05:23 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. Keep out of reach of children, except under adult supervision. If swallowed, get medical help or contact a Poison Control center right away. Do not use in the eyes. Discontinue use if irritation or redness develops. If condition persists, consult a doctor.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.