43742-2260 NDC - BART PLUS (ACONITUM NAPELLUS, APIS MELLIFICA, ARBUTUS ANDRACHNE, ARNICA MONTANA, ARSENICUM ALBUM, COCCULUS INDICUS, ECHINACEA (ANGUSTIFOLIA), GLYCYRRHIZA GLABRA, GUNPOWDER, HEPAR SULPHURIS CALCAREUM, HYDRASTIS CANADENSIS, KALMIA LATIFOLIA, LAC CANINUM, LEDUM PALUSTRE, LYCOPODIUM CLAVATUM, STRAMONIUM, TELLURIUM METALLICUM, THYROIDINUM (SUIS), VERATRUM ALBUM)

Drug Information

  • Product NDC: 43742-2260
  • Proprietary Name: BART PLUS
  • Non Proprietary Name: Aconitum Napellus, Apis Mellifica, Arbutus Andrachne, Arnica Montana, Arsenicum Album, Cocculus Indicus, Echinacea (Angustifolia), Glycyrrhiza Glabra, Gunpowder, Hepar Sulphuris Calcareum, Hydrastis Canadensis, Kalmia Latifolia, Lac Caninum, Ledum Palustre, Lycopodium Clavatum, Stramonium, Tellurium Metallicum, Thyroidinum (Suis), Veratrum Album
  • Active Ingredient(s): 12 [hp_X]/mL ACONITUM NAPELLUS WHOLE; 12 [hp_X]/mL ANAMIRTA COCCULUS SEED; 12 [hp_X]/mL APIS MELLIFERA; 12 [hp_X]/mL ARBUTUS ANDRACHNE LEAFY SHOOT; 3 [hp_X]/mL ARNICA MONTANA WHOLE; 12 [hp_X]/mL ARSENIC TRIOXIDE; 16 [hp_X]/mL CALCIUM SULFIDE; 12 [hp_X]/mL CANIS LUPUS FAMILIARIS MILK; 12 [hp_X]/mL DATURA STRAMONIUM; 3 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE; 6 [hp_X]/mL GLYCYRRHIZA GLABRA; 6 [hp_X]/mL GOLDENSEAL; 12 [hp_X]/mL KALMIA LATIFOLIA LEAF; 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 12 [hp_X]/mL POTASSIUM NITRATE; 6 [hp_X]/mL RHODODENDRON TOMENTOSUM LEAFY TWIG; 16 [hp_X]/mL TELLURIUM; 8 [hp_X]/mL THYROID; 12 [hp_X]/mL VERATRUM ALBUM ROOT
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Standardized Insect Venom Allergenic Extract [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/10/2025

Package Information

No. Package Code Package Description Billing Unit
143742-2260-130 mL in 1 BOTTLE, DROPPER (43742-2260-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-2260The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEBART PLUSThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAconitum Napellus, Apis Mellifica, Arbutus Andrachne, Arnica Montana, Arsenicum Album, Cocculus Indicus, Echinacea (Angustifolia), Glycyrrhiza Glabra, Gunpowder, Hepar Sulphuris Calcareum, Hydrastis Canadensis, Kalmia Latifolia, Lac Caninum, Ledum Palustre, Lycopodium Clavatum, Stramonium, Tellurium Metallicum, Thyroidinum (Suis), Veratrum AlbumThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE3/10/2025This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEDeseret Biologicals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACONITUM NAPELLUS WHOLE; ANAMIRTA COCCULUS SEED; APIS MELLIFERA; ARBUTUS ANDRACHNE LEAFY SHOOT; ARNICA MONTANA WHOLE; ARSENIC TRIOXIDE; CALCIUM SULFIDE; CANIS LUPUS FAMILIARIS MILK; DATURA STRAMONIUM; ECHINACEA ANGUSTIFOLIA WHOLE; GLYCYRRHIZA GLABRA; GOLDENSEAL; KALMIA LATIFOLIA LEAF; LYCOPODIUM CLAVATUM SPORE; POTASSIUM NITRATE; RHODODENDRON TOMENTOSUM LEAFY TWIG; TELLURIUM; THYROID; VERATRUM ALBUM ROOTAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH12; 12; 12; 12; 3; 12; 16; 12; 12; 3; 6; 6; 12; 12; 12; 6; 16; 8; 12 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC] 

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This page was last updated on: 7/4/2025

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