43742-2240 NDC - BIO PLACENTA PHASE (AESCULUS HIPPOCASTANUM, ARTERIA SUIS, ASTRAGALUS EXSCAPUS, BARYTA CARBONICA, CUPRUM SULPHURICUM, DHEA (DEHYDROEPIANDROSTERONE), FUNICULUS UMBILICALIS SUIS, MELILOTUS OFFICINALIS, NATRUM PYRUVICUM, PLACENTA TOTALIS SUIS, PLUMBUM IODATUM, PROTEUS (VULGARIS), QUERCETIN, RUTIN, SARCOLACTICUM ACIDUM, SECALE CORNUTUM, SOLANUM NIGRUM, STROPHANTHUS HISPIDUS, TABACUM, VENA SUIS, VIPERA BERUS)

Drug Information

  • Product NDC: 43742-2240
  • Proprietary Name: Bio Placenta Phase
  • Non Proprietary Name: Aesculus Hippocastanum, Arteria Suis, Astragalus Exscapus, Baryta Carbonica, Cuprum Sulphuricum, DHEA (Dehydroepiandrosterone), Funiculus Umbilicalis Suis, Melilotus Officinalis, Natrum Pyruvicum, Placenta Totalis Suis, Plumbum Iodatum, Proteus (Vulgaris), Quercetin, Rutin, Sarcolacticum Acidum, Secale Cornutum, Solanum Nigrum, Strophanthus Hispidus, Tabacum, Vena Suis, Vipera Berus
  • Active Ingredient(s): 6 [hp_C]/mL ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING; 13 [hp_X]/mL BARIUM CARBONATE; 8 [hp_X]/mL CLAVICEPS PURPUREA SCLEROTIUM; 6 [hp_X]/mL CUPRIC SULFATE; 4 [hp_X]/mL HORSE CHESTNUT; 4 [hp_X]/mL LACTIC ACID, L-; 18 [hp_X]/mL LEAD IODIDE; 6 [hp_X]/mL MELILOTUS OFFICINALIS TOP; 6 [hp_X]/mL PRASTERONE; 30 [hp_C]/mL PROTEUS VULGARIS; 6 [hp_X]/mL QUERCETIN; 6 [hp_X]/mL RUTIN; 8 [hp_X]/mL SODIUM PYRUVATE; 6 [hp_X]/mL SOLANUM NIGRUM WHOLE; 6 [hp_X]/mL STROPHANTHUS HISPIDUS SEED; 10 [hp_X]/mL SUS SCROFA ARTERY; 6 [hp_X]/mL SUS SCROFA PLACENTA; 10 [hp_X]/mL SUS SCROFA UMBILICAL CORD; 8 [hp_X]/mL SUS SCROFA VEIN; 10 [hp_X]/mL TOBACCO LEAF; 20 [hp_X]/mL VIPERA BERUS VENOM
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]

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:11/19/2024

Package Information

No. Package Code Package Description Billing Unit
143742-2240-130 mL in 1 BOTTLE, DROPPER (43742-2240-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-2240The 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 NAMEBio Placenta PhaseThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAesculus Hippocastanum, Arteria Suis, Astragalus Exscapus, Baryta Carbonica, Cuprum Sulphuricum, DHEA (Dehydroepiandrosterone), Funiculus Umbilicalis Suis, Melilotus Officinalis, Natrum Pyruvicum, Placenta Totalis Suis, Plumbum Iodatum, Proteus (Vulgaris), Quercetin, Rutin, Sarcolacticum Acidum, Secale Cornutum, Solanum Nigrum, Strophanthus Hispidus, Tabacum, Vena Suis, Vipera BerusThe 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 DATE11/19/2024This 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 NAMEASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING; BARIUM CARBONATE; CLAVICEPS PURPUREA SCLEROTIUM; CUPRIC SULFATE; HORSE CHESTNUT; LACTIC ACID, L-; LEAD IODIDE; MELILOTUS OFFICINALIS TOP; PRASTERONE; PROTEUS VULGARIS; QUERCETIN; RUTIN; SODIUM PYRUVATE; SOLANUM NIGRUM WHOLE; STROPHANTHUS HISPIDUS SEED; SUS SCROFA ARTERY; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; SUS SCROFA VEIN; TOBACCO LEAF; VIPERA BERUS VENOMAn 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 STRENGTH6; 13; 8; 6; 4; 4; 18; 6; 6; 30; 6; 6; 8; 6; 6; 10; 6; 10; 8; 10; 20 
ACTIVE INGRED UNIT[hp_C]/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_C]/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], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] 

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This page was last updated on: 12/19/2025

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