43742-2263 NDC - GLP SUPPORT (ABIES NIGRA, ABROTANUM (ARTEMISIA ABROTANUM), ANTIMONIUM CRUDUM, BRYONIA (ALBA), CALCAREA PHOSPHORICA, CANTHARIS, CARDUUS MARIANUS, CHELIDONIUM MAJUS, CINCHONA OFFICINALIS, FEL TAURI, IRIS VERSICOLOR, LEDUM PALUSTRE, LYCOPODIUM CLAVATUM, NUX VOMICA, PANCREAS SUIS, PHOSPHORUS, SECALE CORNUTUM)

Drug Information

  • Product NDC: 43742-2263
  • Proprietary Name: GLP Support
  • Non Proprietary Name: Abies Nigra, Abrotanum (Artemisia Abrotanum), Antimonium Crudum, Bryonia (Alba), Calcarea Phosphorica, Cantharis, Carduus Marianus, Chelidonium Majus, Cinchona Officinalis, Fel Tauri, Iris Versicolor, Ledum Palustre, Lycopodium Clavatum, Nux Vomica, Pancreas Suis, Phosphorus, Secale Cornutum
  • Active Ingredient(s): 12 [hp_X]/mL ANTIMONY TRISULFIDE; 12 [hp_X]/mL ARTEMISIA ABROTANUM FLOWERING TOP; 8 [hp_X]/mL BOS TAURUS BILE; 12 [hp_X]/mL BRYONIA ALBA ROOT; 6 [hp_X]/mL CHELIDONIUM MAJUS WHOLE; 12 [hp_X]/mL CINCHONA OFFICINALIS BARK; 12 [hp_X]/mL CLAVICEPS PURPUREA SCLEROTIUM; 12 [hp_X]/mL IRIS VERSICOLOR ROOT; 6 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 12 [hp_X]/mL LYTTA VESICATORIA; 6 [hp_X]/mL MILK THISTLE; 12 [hp_X]/mL PHOSPHORUS; 6 [hp_X]/mL PICEA MARIANA RESIN; 6 [hp_X]/mL RHODODENDRON TOMENTOSUM LEAFY TWIG; 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED; 8 [hp_X]/mL SUS SCROFA PANCREAS; 12 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Blood Coagulation Factor [EPC]; Calcium [CS]; Cations; Divalent [CS]; Cell-mediated Immunity [PE]; Increased Coagulation Factor Activity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Plant Allergenic Extract [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Plant Proteins [CS]; Seed Storage 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:5/7/2025

Package Information

No. Package Code Package Description Billing Unit
143742-2263-130 mL in 1 BOTTLE, DROPPER (43742-2263-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-2263The 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 NAMEGLP SupportThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAbies Nigra, Abrotanum (Artemisia Abrotanum), Antimonium Crudum, Bryonia (Alba), Calcarea Phosphorica, Cantharis, Carduus Marianus, Chelidonium Majus, Cinchona Officinalis, Fel Tauri, Iris Versicolor, Ledum Palustre, Lycopodium Clavatum, Nux Vomica, Pancreas Suis, Phosphorus, Secale CornutumThe 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 DATE5/7/2025This 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 NAMEANTIMONY TRISULFIDE; ARTEMISIA ABROTANUM FLOWERING TOP; BOS TAURUS BILE; BRYONIA ALBA ROOT; CHELIDONIUM MAJUS WHOLE; CINCHONA OFFICINALIS BARK; CLAVICEPS PURPUREA SCLEROTIUM; IRIS VERSICOLOR ROOT; LYCOPODIUM CLAVATUM SPORE; LYTTA VESICATORIA; MILK THISTLE; PHOSPHORUS; PICEA MARIANA RESIN; RHODODENDRON TOMENTOSUM LEAFY TWIG; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA PANCREAS; TRIBASIC CALCIUM PHOSPHATEAn 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; 8; 12; 6; 12; 12; 12; 6; 12; 6; 12; 6; 6; 12; 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 
PHARM CLASSESAllergens [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Plant Proteins [CS], Seed Storage Proteins [CS] 

Download Record

Download this NDC record record in Text format: Export

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

Download this NDC record record in XML format: Export

This page was last updated on: 1/2/2026

Previous Code
Next Code