44911-0419 NDC - LIVEREX I (GINKGO BILOBA, FEL TAURI, GALLBLADDER (SUIS), HEPAR SUIS), THYROIDINUM (SUIS), GERMANIUM SESQUIOXIDE, ALPHA-KETOGLUTARICUM ACIDUM, CITRICUM ACIDUM, FUMARICUM ACIDUM, MALICUM ACIDUM, MANGANUM METALLICUM, PYRUVIC ACID, SUCCINICUM ACIDUM, NAPHTHOCHINONUM, ARSENICUM METALLICUM, SULPHUR, ACONITICUM ACIDUM, CIS, LYCOPODIUM CLAVATUM, NATRUM OXALACETICUM, PHOSPHORUS)

Drug Information

  • Product NDC: 44911-0419
  • Proprietary Name: Liverex I
  • Non Proprietary Name: Ginkgo Biloba, Fel Tauri, Gallbladder (Suis), Hepar Suis), Thyroidinum (Suis), Germanium Sesquioxide, Alpha-Ketoglutaricum Acidum, Citricum Acidum, Fumaricum Acidum, Malicum Acidum, Manganum Metallicum, Pyruvic Acid, Succinicum Acidum, Naphthochinonum, Arsenicum Metallicum, Sulphur, Aconiticum Acidum, Cis, Lycopodium Clavatum, Natrum Oxalaceticum, Phosphorus
  • Active Ingredient(s): 9 [hp_X]/mL 1,4-NAPHTHOQUINONE; 12 [hp_X]/mL ACONITIC ACID, (Z)-; 8 [hp_X]/mL ANHYDROUS CITRIC ACID; 12 [hp_X]/mL ARSENIC; 6 [hp_X]/mL BOS TAURUS BILE; 8 [hp_X]/mL FUMARIC ACID; 8 [hp_X]/mL GERMANIUM SESQUIOXIDE; 6 [hp_X]/mL GINKGO; 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 8 [hp_X]/mL MALIC ACID; 8 [hp_X]/mL MANGANESE; 8 [hp_X]/mL OXOGLURIC ACID; 12 [hp_X]/mL PHOSPHORUS; 6 [hp_X]/mL PORK LIVER; 8 [hp_X]/mL PYRUVIC ACID; 12 [hp_X]/mL SODIUM DIETHYL OXALACETATE; 8 [hp_X]/mL SUCCINIC ACID; 12 [hp_X]/mL SULFUR; 6 [hp_X]/mL SUS SCROFA GALLBLADDER; 6 [hp_X]/mL THYROID
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Acidifying Activity [MoA]; Anti-coagulant [EPC]; Calcium Chelating Activity [MoA]; Calculi Dissolution Agent [EPC]; Decreased Coagulation Factor Activity [PE]

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:2/28/2017

Package Information

No. Package Code Package Description Billing Unit
144911-0419-130 mL in 1 BOTTLE, DROPPER (44911-0419-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC44911-0419The 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 NAMELiverex IThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEGinkgo Biloba, Fel Tauri, Gallbladder (Suis), Hepar Suis), Thyroidinum (Suis), Germanium Sesquioxide, Alpha-Ketoglutaricum Acidum, Citricum Acidum, Fumaricum Acidum, Malicum Acidum, Manganum Metallicum, Pyruvic Acid, Succinicum Acidum, Naphthochinonum, Arsenicum Metallicum, Sulphur, Aconiticum Acidum, Cis, Lycopodium Clavatum, Natrum Oxalaceticum, PhosphorusThe 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 DATE2/28/2017This 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 NAME1,4-NAPHTHOQUINONE; ACONITIC ACID, (Z)-; ANHYDROUS CITRIC ACID; ARSENIC; BOS TAURUS BILE; FUMARIC ACID; GERMANIUM SESQUIOXIDE; GINKGO; LYCOPODIUM CLAVATUM SPORE; MALIC ACID; MANGANESE; OXOGLURIC ACID; PHOSPHORUS; PORK LIVER; PYRUVIC ACID; SODIUM DIETHYL OXALACETATE; SUCCINIC ACID; SULFUR; SUS SCROFA GALLBLADDER; THYROIDAn 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; 12; 8; 12; 6; 8; 8; 6; 12; 8; 8; 8; 12; 6; 8; 12; 8; 12; 6; 6 
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 
PHARM CLASSESAcidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE] 

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This page was last updated on: 12/6/2025

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