43742-1537 NDC - LIVER DRAINAGE (CHELIDONIUM MAJUS, CARDUUS MARIANUS, SCHISANDRA CHINENSIS, TARAXACUM OFFICINALE, BERBERIS VULGARIS, NEOPICRORHIZA SCROPHULARIIFLORA, RAPHANUS SATIVUS, VISCUM ALBUM, CHROMIUM PICOLINATE, COBALT GLUCONATE, COPPER GLUCONATE, MAGNESIUM GLUCONATE, NATRUM SULPHURICUM, PTELEA TRIFOLIATE, SARCOLACTICUM ACIDUM, SULPHUR IODATUM, CARBOLICUM ACIDUM, CICHORIUM INTYBUS, FLOS, GALLBLADDER (SUIS), HEPAR SUIS, NUX VOMICA, PANCREAS SUIS, VANADIUM METALLICUM, VERBENA OFFICINALIS, FLOS)

Drug Information

Product NDC: 43742-1537

Proprietary Name: Liver Drainage

Non Proprietary Name: Chelidonium Majus, Carduus Marianus, Schisandra Chinensis, Taraxacum Officinale, Berberis Vulgaris, Neopicrorhiza Scrophulariiflora, Raphanus Sativus, Viscum Album, Chromium Picolinate, Cobalt Gluconate, Copper Gluconate, Magnesium Gluconate, Natrum Sulphuricum, Ptelea Trifoliate, Sarcolacticum Acidum, Sulphur Iodatum, Carbolicum Acidum, Cichorium Intybus, Flos, Gallbladder (Suis), Hepar Suis, Nux Vomica, Pancreas Suis, Vanadium Metallicum, Verbena Officinalis, Flos

Active Ingredient(s):
  • 3 [hp_X]/mL BERBERIS VULGARIS ROOT BARK;
  • 1 [hp_X]/mL CHELIDONIUM MAJUS;
  • 6 [hp_X]/mL CHROMIUM PICOLINATE;
  • 8 [hp_X]/mL CICHORIUM INTYBUS FLOWER;
  • 6 [hp_X]/mL COBALTOUS GLUCONATE;
  • 6 [hp_X]/mL COPPER GLUCONATE;
  • 6 [hp_X]/mL LACTIC ACID, L-;
  • 6 [hp_X]/mL MAGNESIUM GLUCONATE;
  • 2 [hp_X]/mL MILK THISTLE;
  • 3 [hp_X]/mL NEOPICRORHIZA SCROPHULARIIFLORA ROOT;
  • 8 [hp_X]/mL PHENOL;
  • 8 [hp_X]/mL PORK LIVER;
  • 6 [hp_X]/mL PTELEA TRIFOLIATA BARK;
  • 3 [hp_X]/mL RADISH;
  • 2 [hp_X]/mL SCHISANDRA CHINENSIS FRUIT;
  • 6 [hp_X]/mL SODIUM SULFATE;
  • 8 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED;
  • 6 [hp_X]/mL SULFUR IODIDE;
  • 8 [hp_X]/mL SUS SCROFA GALLBLADDER;
  • 8 [hp_X]/mL SUS SCROFA PANCREAS;
  • 2 [hp_X]/mL TARAXACUM OFFICINALE;
  • 8 [hp_X]/mL VANADIUM;
  • 8 [hp_X]/mL VERBENA OFFICINALIS FLOWERING TOP;
  • 3 [hp_X]/mL VISCUM ALBUM FRUITING TOP


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Allergens [CS];
  • Calculi Dissolution Agent [EPC];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Increased Large Intestinal Motility [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE];
  • Magnesium Ion Exchange Activity [MoA];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Plant Proteins [CS];
  • Seed Storage Proteins [CS];
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE];
  • Vegetable Proteins [CS]

Labeler Information

Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/22/2019
End Marketing Date:4/1/2026

Package Information

No. Package Code Package Description Billing Unit
143742-1537-160 mL in 1 BOTTLE, DROPPER (43742-1537-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1537The 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 NAMELiver DrainageThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEChelidonium Majus, Carduus Marianus, Schisandra Chinensis, Taraxacum Officinale, Berberis Vulgaris, Neopicrorhiza Scrophulariiflora, Raphanus Sativus, Viscum Album, Chromium Picolinate, Cobalt Gluconate, Copper Gluconate, Magnesium Gluconate, Natrum Sulphuricum, Ptelea Trifoliate, Sarcolacticum Acidum, Sulphur Iodatum, Carbolicum Acidum, Cichorium Intybus, Flos, Gallbladder (Suis), Hepar Suis, Nux Vomica, Pancreas Suis, Vanadium Metallicum, Verbena Officinalis, FlosThe 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 DATE8/22/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE4/1/2026This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
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 NAMEBERBERIS VULGARIS ROOT BARK; CHELIDONIUM MAJUS; CHROMIUM PICOLINATE; CICHORIUM INTYBUS FLOWER; COBALTOUS GLUCONATE; COPPER GLUCONATE; LACTIC ACID, L-; MAGNESIUM GLUCONATE; MILK THISTLE; NEOPICRORHIZA SCROPHULARIIFLORA ROOT; PHENOL; PORK LIVER; PTELEA TRIFOLIATA BARK; RADISH; SCHISANDRA CHINENSIS FRUIT; SODIUM SULFATE; STRYCHNOS NUX-VOMICA SEED; SULFUR IODIDE; SUS SCROFA GALLBLADDER; SUS SCROFA PANCREAS; TARAXACUM OFFICINALE; VANADIUM; VERBENA OFFICINALIS FLOWERING TOP; VISCUM ALBUM FRUITING TOPAn 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 STRENGTH3; 1; 6; 8; 6; 6; 6; 6; 2; 3; 8; 8; 6; 3; 2; 6; 8; 6; 8; 8; 2; 8; 8; 3 
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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vegetable Proteins [CS] 

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023