43742-1564 NDC - KIDNEY DRAINAGE (SOLIDAGO VIRGAUREA, ASPARAGUS OFFICINALIS, JUNIPERUS COMMUNIS, SABAL SERRULATA, UVA-URSI, BERBERIS VULGARIS, EQUISETUM ARVENSE, URTICA DIOICA, RUBIA TINCTORUM, STAPHYSAGRIA, CANTHARIS, FAGUS SYLVATICA, FLOS, GLANDULA SUPRARENALIS SUIS, HEPAR SULPHURIS CALCAREUM, KIDNEY (SUIS), LARIX DECIDUA, FLOS, MANGANUM METALLICUM, MIMULUS GUTTATUS, FLOS, NITRICUM ACIDUM, RHUS AROMATICA, SILICEA, ULEX EUROPAEUS, FLOS, BENZOICUM ACIDUM, COBALTUM METALLICUM)

Drug Information

Product NDC: 43742-1564

Proprietary Name: Kidney Drainage

Non Proprietary Name: Solidago Virgaurea, Asparagus Officinalis, Juniperus Communis, Sabal Serrulata, Uva-Ursi, Berberis Vulgaris, Equisetum Arvense, Urtica Dioica, Rubia Tinctorum, Staphysagria, Cantharis, Fagus Sylvatica, Flos, Glandula Suprarenalis Suis, Hepar Sulphuris Calcareum, Kidney (Suis), Larix Decidua, Flos, Manganum Metallicum, Mimulus Guttatus, Flos, Nitricum Acidum, Rhus Aromatica, Silicea, Ulex Europaeus, Flos, Benzoicum Acidum, Cobaltum Metallicum

Active Ingredient(s):
  • 2 [hp_X]/mL ARCTOSTAPHYLOS UVA-URSI LEAF;
  • 2 [hp_X]/mL ASPARAGUS;
  • 12 [hp_X]/mL BENZOIC ACID;
  • 3 [hp_X]/mL BERBERIS VULGARIS ROOT BARK;
  • 8 [hp_X]/mL CALCIUM SULFIDE;
  • 16 [hp_X]/mL COBALT;
  • 6 [hp_X]/mL DELPHINIUM STAPHISAGRIA SEED;
  • 3 [hp_X]/mL EQUISETUM ARVENSE TOP;
  • 8 [hp_X]/mL FAGUS SYLVATICA FLOWERING TOP;
  • 2 [hp_X]/mL JUNIPERUS COMMUNIS WHOLE;
  • 8 [hp_X]/mL LARIX DECIDUA FLOWERING TOP;
  • 8 [hp_X]/mL LYTTA VESICATORIA;
  • 8 [hp_X]/mL MANGANESE;
  • 8 [hp_X]/mL MIMULUS GUTTATUS FLOWERING TOP;
  • 8 [hp_X]/mL NITRIC ACID;
  • 8 [hp_X]/mL PORK KIDNEY;
  • 8 [hp_X]/mL RHUS AROMATICA ROOT BARK;
  • 6 [hp_X]/mL RUBIA TINCTORUM ROOT;
  • 2 [hp_X]/mL SAW PALMETTO;
  • 8 [hp_X]/mL SILICON DIOXIDE;
  • 1 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP;
  • 8 [hp_X]/mL SUS SCROFA ADRENAL GLAND;
  • 8 [hp_X]/mL ULEX EUROPAEUS FLOWER;
  • 3 [hp_X]/mL URTICA DIOICA


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Allergens [CS];
  • Ammonium Ion Binding Activity [MoA];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Nitrogen Binding Agent [EPC];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Standardized Chemical Allergen [EPC];
  • Vegetable Proteins [CS]

Labeler Information

Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/17/2019

Package Information

No. Package Code Package Description Billing Unit
143742-1564-160 mL in 1 BOTTLE, DROPPER (43742-1564-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1564The 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 PRESCRIPTION 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 NAMEKidney 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 NAMESolidago Virgaurea, Asparagus Officinalis, Juniperus Communis, Sabal Serrulata, Uva-Ursi, Berberis Vulgaris, Equisetum Arvense, Urtica Dioica, Rubia Tinctorum, Staphysagria, Cantharis, Fagus Sylvatica, Flos, Glandula Suprarenalis Suis, Hepar Sulphuris Calcareum, Kidney (Suis), Larix Decidua, Flos, Manganum Metallicum, Mimulus Guttatus, Flos, Nitricum Acidum, Rhus Aromatica, Silicea, Ulex Europaeus, Flos, Benzoicum Acidum, Cobaltum MetallicumThe 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 DATE9/17/2019This 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 NAMEARCTOSTAPHYLOS UVA-URSI LEAF; ASPARAGUS; BENZOIC ACID; BERBERIS VULGARIS ROOT BARK; CALCIUM SULFIDE; COBALT; DELPHINIUM STAPHISAGRIA SEED; EQUISETUM ARVENSE TOP; FAGUS SYLVATICA FLOWERING TOP; JUNIPERUS COMMUNIS WHOLE; LARIX DECIDUA FLOWERING TOP; LYTTA VESICATORIA; MANGANESE; MIMULUS GUTTATUS FLOWERING TOP; NITRIC ACID; PORK KIDNEY; RHUS AROMATICA ROOT BARK; RUBIA TINCTORUM ROOT; SAW PALMETTO; SILICON DIOXIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; SUS SCROFA ADRENAL GLAND; ULEX EUROPAEUS FLOWER; URTICA DIOICAAn 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 STRENGTH2; 2; 12; 3; 8; 16; 6; 3; 8; 2; 8; 8; 8; 8; 8; 8; 8; 6; 2; 8; 1; 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], Ammonium Ion Binding Activity [MoA], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Nitrogen Binding Agent [EPC], Non-Standardized Food Allergenic Extract [EPC], Standardized Chemical Allergen [EPC], 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