Home FDA labels 0bca210b-fcd7-9c55-e063-6294a90ace85 FDA label 0bca210b-fcd7-9c55-e063-6294a90ace85 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 7d6166ad-2227-4f9b-b6da-b85a6e124d75
SPL ID 0bca210b-fcd7-9c55-e063-6294a90ace85
Version 5
Effective date 2023-12-05
Source export date 2026-11-06
Source partition 1
Source file https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run 20261108T063105Z
Imported at 2026-11-08 06:42:49 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 in eyes, on deep puncture wounds, animal bites, or serious burns or for more than 1 week unless directed by a doctor. Stop use and ask a doctor if: A rash or allergic reaction develops. Condition worsens, persists, or recurs.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.