Home FDA labels 0cdb270f-83ca-9a4f-e063-6394a90a6b6b FDA label 0cdb270f-83ca-9a4f-e063-6394a90a6b6b 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 18d4f5f7-a4cd-7425-e054-00144ff88e88
SPL ID 0cdb270f-83ca-9a4f-e063-6394a90a6b6b
Version 3
Effective date 2023-12-19
Source export date 2026-11-06
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/10387d7618367cd955339e75d48af3d11f99f789153db05c529d9fad6eccc645/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run 20261108T063105Z
Imported at 2026-11-08 07:19:29 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 OTC- Warnings Section For external use only When using this product • do not get into eyes. Do not use if you are allergic to plants of the Asteraceae/Compositae/ Daisy family. Hypersensitivity, such as allergy, has been known to occur; in which case, discontinue use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.