Home FDA labels 4af75847-5944-45b7-95d6-efa3369c29ab Food Additives 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 Food Additives
Generic name BERBERIS VULGARIS, CHELIDONIUM MAJUS, TRIFOLIUM PRATENSE, GLYCYRRHIZA GLABRA, LAPPA MAJOR, PHYTOLACCA DECANDRA, RHAMNUS FRANGULA, RHAMNUS PURSHIANA, STILLINGIA SYLVATICA, XANTHOXYLUM FRAXINEUM, ARSENICUM ALBUM, BELLADONNA, LYCOPODIUM CLAVATUM, NATRUM SULPHURICUM, PHOSPHORICUM ACIDUM
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID bf27d457-12e1-4ab6-b132-1b65cde0ed93
SPL ID 4af75847-5944-45b7-95d6-efa3369c29ab
Version 2
Effective date 2016-09-28
Source export date 2026-09-28
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:40:38 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Food Additives openfda.brand_name generic name BERBERIS VULGARIS, CHELIDONIUM MAJUS, TRIFOLIUM PRATENSE, GLYCYRRHIZA GLABRA, LAPPA MAJOR, PHYTOLACCA DECANDRA, RHAMNUS FRANGULA, RHAMNUS PURSHIANA, STILLINGIA SYLVATICA, XANTHOXYLUM FRAXINEUM, ARSENICUM ALBUM, BELLADONNA, LYCOPODIUM CLAVATUM, NATRUM SULPHURICUM, PHOSPHORICUM ACIDUM openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0168-1 openfda.package_ndc ndc product 43857-0168 openfda.product_ndc ndc11 package 43857016801 derived:openfda.package_ndc spl id 4af75847-5944-45b7-95d6-efa3369c29ab id spl set id bf27d457-12e1-4ab6-b132-1b65cde0ed93 set_id unii 11E6VI8VEG openfda.unii unii 7E889U5RNN openfda.unii unii 2788Z9758H openfda.unii unii A4KL1HMZ7T openfda.unii unii S2D77IH61R openfda.unii unii 0YPR65R21J openfda.unii unii 1TH8Q20J0U openfda.unii unii 4VBP01X99F openfda.unii unii DSV74G1P2J openfda.unii unii S7V92P67HO openfda.unii unii E4GA8884NN openfda.unii unii QBR70R4FBK openfda.unii unii 4JS0838828 openfda.unii unii C88X29Y479 openfda.unii unii 597E9BI3Z3 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: If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.