44911-0679 NDC - LIVER GALLBLADDER (BELLADONNA, CARDUUS MARIANUS, CHELIDONIUM MAJUS, CHIONANTHUS VIRGINICA, CINCHONA OFFICINALIS, COLOCYNTHIS, LEPTANDRA VIRGINICA, LYCOPODIUM CLAVATUM, NATRUM SULPHURICUM, NUX VOMICA, PHOSPHORUS, PTELEA TRIFOLIATA, PULSATILLA (PRATENSIS), VERATRUM ALBUM)

Drug Information

  • Product NDC: 44911-0679
  • Proprietary Name: Liver Gallbladder
  • Non Proprietary Name: Belladonna, Carduus Marianus, Chelidonium Majus, Chionanthus Virginica, Cinchona Officinalis, Colocynthis, Leptandra Virginica, Lycopodium Clavatum, Natrum Sulphuricum, Nux Vomica, Phosphorus, Ptelea Trifoliata, Pulsatilla (Pratensis), Veratrum Album
  • Active Ingredient(s): 30 [hp_X]/mL ATROPA BELLADONNA; 30 [hp_X]/mL CHELIDONIUM MAJUS WHOLE; 30 [hp_X]/mL CHIONANTHUS VIRGINICUS ROOT BARK; 30 [hp_X]/mL CINCHONA OFFICINALIS BARK; 30 [hp_X]/mL CITRULLUS COLOCYNTHIS FRUIT PULP; 30 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 30 [hp_X]/mL MILK THISTLE; 30 [hp_X]/mL PHOSPHORUS; 30 [hp_X]/mL PTELEA TRIFOLIATA BARK; 30 [hp_X]/mL PULSATILLA PRATENSIS WHOLE; 30 [hp_X]/mL SODIUM SULFATE; 30 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED; 30 [hp_X]/mL VERATRUM ALBUM ROOT; 30 [hp_X]/mL VERONICASTRUM VIRGINICUM ROOT
  • 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]; Seed Storage Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: Energique, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/4/2023

Package Information

No. Package Code Package Description Billing Unit
144911-0679-130 mL in 1 BOTTLE, DROPPER (44911-0679-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC44911-0679The 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 GallbladderThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXHPA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
NON PROPRIETARY NAMEBelladonna, Carduus Marianus, Chelidonium Majus, Chionanthus Virginica, Cinchona Officinalis, Colocynthis, Leptandra Virginica, Lycopodium Clavatum, Natrum Sulphuricum, Nux Vomica, Phosphorus, Ptelea Trifoliata, Pulsatilla (Pratensis), Veratrum AlbumThe 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 DATE8/4/2023This 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 NAMEEnergique, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEATROPA BELLADONNA; CHELIDONIUM MAJUS WHOLE; CHIONANTHUS VIRGINICUS ROOT BARK; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; LYCOPODIUM CLAVATUM SPORE; MILK THISTLE; PHOSPHORUS; PTELEA TRIFOLIATA BARK; PULSATILLA PRATENSIS WHOLE; SODIUM SULFATE; STRYCHNOS NUX-VOMICA SEED; VERATRUM ALBUM ROOT; VERONICASTRUM VIRGINICUM ROOTAn 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 STRENGTH30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 
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 
PHARM CLASSESAllergens [CS], 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] 

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: 11/21/2025

Previous Code
Next Code