Home FDA labels ed10aff6-7a4c-4115-e053-2995a90a9d1a UNDA 43 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 43
Generic name ALUMINIUM METALLICUM, ASPERULA ODORATA, EQUISETUM ARVENSE, JATEORHIZA PALMATA, MARRUBIUM VULGARE, OCIMUM BASILICUM, STANNUM METALLICUM
Manufacturer Seroyal USA
Product type HUMAN OTC DRUG
SPL set ID 20569964-d505-03e2-e054-00144ff8d46c
SPL ID ed10aff6-7a4c-4115-e053-2995a90a9d1a
Version 5
Effective date 2022-11-09
Source export date 2026-09-28
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:18:37 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 · 27 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name UNDA 43 openfda.brand_name brand name UNDA 47 openfda.brand_name generic name ABSINTHIUM, ARNICA MONTANA, AURUM METALLICUM, JATEORHIZA PALMATA, ROSMARINUS OFFICINALIS, STIBIUM METALLICUM, THYMUS VULGARIS, VALERIANA OFFICINALIS openfda.generic_name generic name ALUMINIUM METALLICUM, ASPERULA ODORATA, EQUISETUM ARVENSE, JATEORHIZA PALMATA, MARRUBIUM VULGARE, OCIMUM BASILICUM, STANNUM METALLICUM openfda.generic_name manufacturer name Seroyal USA openfda.manufacturer_name ndc package 62106-1146-8 openfda.package_ndc ndc package 62106-1142-8 openfda.package_ndc ndc product 62106-1146 openfda.product_ndc ndc product 62106-1142 openfda.product_ndc ndc11 package 62106114608 derived:openfda.package_ndc ndc11 package 62106114208 derived:openfda.package_ndc spl id ed10aff6-7a4c-4115-e053-2995a90a9d1a id spl set id 20569964-d505-03e2-e054-00144ff8d46c set_id unii 387GMG9FH5 openfda.unii unii 9IT35J3UV3 openfda.unii unii IJ67X351P9 openfda.unii unii F84709P2XV openfda.unii unii N8C4A9A49H openfda.unii unii 79Y1949PYO openfda.unii unii 2U0KZP0FDW openfda.unii unii 7A72MUN24Z openfda.unii unii JWF5YAW3QW openfda.unii unii 8L72OKJ7II openfda.unii unii CPD4NFA903 openfda.unii unii V36I2B8LD5 openfda.unii unii 1DP6Y6B65Z openfda.unii unii MUE8Y11327 openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 2 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.
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.