Home FDA labels ecfa9109-e935-ad4e-e053-2a95a90a372b Unda 11 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 11
Generic name ASPARAGUS OFFICINALIS YOUNG SHOOT, MENTHA PIPERITA WHOLE PLANT, MILLEFOLIUM WHOLE PLANT,THYMUS SERPYLLUM WHOLE PLANT, CROCUS SATIVUS DRIED STIGMA, ROSMARINUS OFFICINALIS FLOWERING TWIGS, GLECHOMA HEDERACEA WHOLE PLANT, VERBENA OFFICINALIS WHOLE PLANT, UVA-URSI LEAF, CUPRUM METALLICUM
Manufacturer Seroyal USA
Product type HUMAN OTC DRUG
SPL set ID 0fd85527-b04b-3f4a-e054-00144ff8d46c
SPL ID ecfa9109-e935-ad4e-e053-2a95a90a372b
Version 5
Effective date 2022-11-08
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 06:18:14 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 · 18 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Unda 11 openfda.brand_name generic name ASPARAGUS OFFICINALIS YOUNG SHOOT, MENTHA PIPERITA WHOLE PLANT, MILLEFOLIUM WHOLE PLANT,THYMUS SERPYLLUM WHOLE PLANT, CROCUS SATIVUS DRIED STIGMA, ROSMARINUS OFFICINALIS FLOWERING TWIGS, GLECHOMA HEDERACEA WHOLE PLANT, VERBENA OFFICINALIS WHOLE PLANT, UVA-URSI LEAF, CUPRUM METALLICUM openfda.generic_name manufacturer name Seroyal USA openfda.manufacturer_name ndc package 62106-1110-8 openfda.package_ndc ndc product 62106-1110 openfda.product_ndc ndc11 package 62106111008 derived:openfda.package_ndc spl id ecfa9109-e935-ad4e-e053-2a95a90a372b id spl set id 0fd85527-b04b-3f4a-e054-00144ff8d46c set_id unii 2FXJ6SW4PK openfda.unii unii QT8A71T9BM openfda.unii unii 86H4S6K51N openfda.unii unii 79M2M2UDA9 openfda.unii unii 789U1901C5 openfda.unii unii Z1EJP3037Z openfda.unii unii 8JM482TI79 openfda.unii unii L6O7WQK912 openfda.unii unii 3M5V3D1X36 openfda.unii unii E849G4X5YJ openfda.unii
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.