43742-1171 NDC - H. PYLORI PLUS (ANGELICA ARCHANGELICA, GERANIUM MACULATUM, HYDRASTIS CANADENSIS, SINAPIS NIGRA, SYMPHYTUM OFFICINALE, RATANHIA, ACETICUM ACIDUM, CARBOLICUM ACIDUM, ORNITHOGALUM UMBELLATUM, ABIES CANADENSIS, ANACARDIUM ORIENTALE, BISMUTHUM SUBNITRICUM, CONDURANGO, GRAPHITES, IRIS VERSICOLOR, LYCOPODIUM CLAVATUM, MEZEREUM, URANIUM NITRICUM, EUPHORBIUM OFFICINARUM, NUX VOMICA)

Drug Information

Product NDC: 43742-1171

Proprietary Name: H. Pylori Plus

Non Proprietary Name: Angelica Archangelica, Geranium Maculatum, Hydrastis Canadensis, Sinapis Nigra, Symphytum Officinale, Ratanhia, Aceticum Acidum, Carbolicum Acidum, Ornithogalum Umbellatum, Abies Canadensis, Anacardium Orientale, Bismuthum Subnitricum, Condurango, Graphites, Iris Versicolor, Lycopodium Clavatum, Mezereum, Uranium Nitricum, Euphorbium Officinarum, Nux Vomica

Active Ingredient(s):
  • 9 [hp_X]/mL ACETIC ACID;
  • 6 [hp_X]/mL ANGELICA ARCHANGELICA ROOT;
  • 12 [hp_X]/mL BISMUTH SUBNITRATE;
  • 6 [hp_X]/mL BLACK MUSTARD SEED;
  • 6 [hp_X]/mL COMFREY ROOT;
  • 12 [hp_X]/mL DAPHNE MEZEREUM BARK;
  • 12 [hp_X]/mL EUPHORBIA RESINIFERA RESIN;
  • 6 [hp_X]/mL GERANIUM MACULATUM ROOT;
  • 6 [hp_X]/mL GOLDENSEAL;
  • 12 [hp_X]/mL GRAPHITE;
  • 12 [hp_X]/mL IRIS VERSICOLOR ROOT;
  • 6 [hp_X]/mL KRAMERIA LAPPACEA ROOT;
  • 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE;
  • 12 [hp_X]/mL MARSDENIA CONDURANGO BARK;
  • 10 [hp_X]/mL ORNITHOGALUM UMBELLATUM;
  • 9 [hp_X]/mL PHENOL;
  • 12 [hp_X]/mL SEMECARPUS ANACARDIUM JUICE;
  • 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED;
  • 10 [hp_X]/mL TSUGA CANADENSIS BARK;
  • 10 [hp_X]/mL TSUGA CANADENSIS FLOWER BUD;
  • 12 [hp_X]/mL URANYL NITRATE HEXAHYDRATE


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Bismuth [CS];
  • Bismuth [EPC];
  • Cell-mediated Immunity [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Plant Proteins [CS];
  • Seed Storage Proteins [CS]

Labeler Information

Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/6/2018
End Marketing Date:7/20/2025

Package Information

No. Package Code Package Description Billing Unit
143742-1171-130 mL in 1 BOTTLE, DROPPER (43742-1171-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1171The 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 NAMEH. Pylori 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 NAMEAngelica Archangelica, Geranium Maculatum, Hydrastis Canadensis, Sinapis Nigra, Symphytum Officinale, Ratanhia, Aceticum Acidum, Carbolicum Acidum, Ornithogalum Umbellatum, Abies Canadensis, Anacardium Orientale, Bismuthum Subnitricum, Condurango, Graphites, Iris Versicolor, Lycopodium Clavatum, Mezereum, Uranium Nitricum, Euphorbium Officinarum, Nux VomicaThe 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 DATE3/6/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE7/20/2025This 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 NAMEACETIC ACID; ANGELICA ARCHANGELICA ROOT; BISMUTH SUBNITRATE; BLACK MUSTARD SEED; COMFREY ROOT; DAPHNE MEZEREUM BARK; EUPHORBIA RESINIFERA RESIN; GERANIUM MACULATUM ROOT; GOLDENSEAL; GRAPHITE; IRIS VERSICOLOR ROOT; KRAMERIA LAPPACEA ROOT; LYCOPODIUM CLAVATUM SPORE; MARSDENIA CONDURANGO BARK; ORNITHOGALUM UMBELLATUM; PHENOL; SEMECARPUS ANACARDIUM JUICE; STRYCHNOS NUX-VOMICA SEED; TSUGA CANADENSIS BARK; TSUGA CANADENSIS FLOWER BUD; URANYL NITRATE HEXAHYDRATEAn 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 STRENGTH9; 6; 12; 6; 6; 12; 12; 6; 6; 12; 12; 6; 12; 12; 10; 9; 12; 12; 10; 10; 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; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Bismuth [CS], Bismuth [EPC], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS] 

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