Home FDA labels ed11e5b0-cdb0-1f9a-e053-2995a90a0f16 UNDA 240 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)
Brand name UNDA 240
Generic name EQUISETUM ARVENSE, GENTIANA LUTEA, SALVIA OFFICINALIS, SAXIFRAGA GRANULATA, SPIRAEA ULMARIA
Manufacturer Seroyal USA
Product type HUMAN OTC DRUG
SPL set ID 43a3d9da-f7e9-2257-e054-00144ff8d46c
SPL ID ed11e5b0-cdb0-1f9a-e053-2995a90a0f16
Version 3
Effective date 2022-11-09
Source export date 2026-10-27
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/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run 20261027T193451Z
Imported at 2026-10-27 20:16:15 Harmonized routes table Harmonized routes ORAL
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 · 13 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 Stop use and ask a doctor if symptoms persist or worsen. If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.