Home FDA labels bf8c654d-5f17-4d2b-bf5b-421ae49ab6e4 BART PLUS 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 BART PLUS
Generic name ARNICA MONTANA, ECHINACEA (ANGUSTIFOLIA), GLYCYRRHIZA GLABRA, HYDRASTIS CANADENSIS, LEDUM PALUSTRE, THYROIDINUM (SUIS), ARBUTUS ANDRACHNE, APIS MELLIFICA, ARSENICUM ALBUM, COCCULUS INDICUS, GUNPOWDER, HEPAR SULPHURIS CALCAREUM, KALMIA LATIFOLIA, LAC CANINUM, LYCOPODIUM CLAVATUM, VERATRUM ALBUM, ACONITUM NAPELLUS, STRAMONIUM, TELLURIUM METALLICUM
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID ffdaf5a6-6174-425e-81e1-8c8149b9e547
SPL ID bf8c654d-5f17-4d2b-bf5b-421ae49ab6e4
Version 4
Effective date 2024-10-04
Source export date 2026-09-28
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:56:02 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 BART PLUS openfda.brand_name generic name ARNICA MONTANA, ECHINACEA (ANGUSTIFOLIA), GLYCYRRHIZA GLABRA, HYDRASTIS CANADENSIS, LEDUM PALUSTRE, THYROIDINUM (SUIS), ARBUTUS ANDRACHNE, APIS MELLIFICA, ARSENICUM ALBUM, COCCULUS INDICUS, GUNPOWDER, HEPAR SULPHURIS CALCAREUM, KALMIA LATIFOLIA, LAC CANINUM, LYCOPODIUM CLAVATUM, VERATRUM ALBUM, ACONITUM NAPELLUS, STRAMONIUM, TELLURIUM METALLICUM openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-1701-1 openfda.package_ndc ndc product 43742-1701 openfda.product_ndc ndc11 package 43742170101 derived:openfda.package_ndc spl id bf8c654d-5f17-4d2b-bf5b-421ae49ab6e4 id spl set id ffdaf5a6-6174-425e-81e1-8c8149b9e547 set_id unii 2P3VWU3H10 openfda.unii unii 6RV024OAUQ openfda.unii unii 877L01IZ0P openfda.unii unii 2788Z9758H openfda.unii unii O80TY208ZW openfda.unii unii 79N6542N18 openfda.unii unii G39P120JQT openfda.unii unii S7V92P67HO openfda.unii unii VB06AV5US8 openfda.unii unii ZW3Z11D0JV openfda.unii unii U0NQ8555JD openfda.unii unii G6W4F0V8Z3 openfda.unii unii 810258W28U openfda.unii unii 7S82P3R43Z openfda.unii unii NQA0O090ZJ openfda.unii unii QNS6W5US1Z openfda.unii unii C88X29Y479 openfda.unii unii 72QQ293E8P openfda.unii unii 1MBW07J51Q 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 professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.