Liverex I Liquid
NDC 44911-0419

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0419?
  4. Liverex I Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

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) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Energique, Inc.. This medication is typically used as a acidifying activity [moa]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 44911-0419 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
44911-0419
Proprietary Name:
Liverex I
Non-Proprietary Name: [1]
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
Substance Name: [2]
1,4-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; Thyroid
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Energique, Inc.
Labeler Code:
44911
Product Label ID:
1c23c489-0a43-4736-a30a-0ae02c09fb45
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
02-28-2017
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 44911-0419?

The NDC code 44911-0419 is assigned by the FDA to the product Liverex I. It is commonly known by its generic 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. This pharmaceutical product is labeled by Energique, Inc. and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 44911-0419-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Liver, Gallbladder support.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration. Liver, Gallbladder support.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

What are Active Ingredients of this product?

An 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.
  • 1,4-NAPHTHOQUINONE 9 [hp_X]/mL
  • ACONITIC ACID, (Z)- 12 [hp_X]/mL
  • ANHYDROUS CITRIC ACID 8 [hp_X]/mL - A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.
  • ARSENIC 12 [hp_X]/mL - A shiny gray element with atomic symbol As, atomic number 33, and atomic weight 75. It occurs throughout the universe, mostly in the form of metallic arsenides. Most forms are toxic. According to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985), arsenic and certain arsenic compounds have been listed as known carcinogens. (From Merck Index, 11th ed)
  • BOS TAURUS BILE 6 [hp_X]/mL
  • FUMARIC ACID 8 [hp_X]/mL - see also record for ferrous fumarate; use FUMARATES for general fumaric acid esters
  • GERMANIUM SESQUIOXIDE 8 [hp_X]/mL
  • GINKGO 6 [hp_X]/mL - The only specie of the genus Ginkgo, family Ginkgoacea. It is the source of extracts of medicinal interest, especially Egb 761. Ginkgo may refer to the genus or species.
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • MALIC ACID 8 [hp_X]/mL
  • MANGANESE 8 [hp_X]/mL - A trace element with atomic symbol Mn, atomic number 25, and atomic weight 54.94. It is concentrated in cell mitochondria, mostly in the pituitary gland, liver, pancreas, kidney, and bone, influences the synthesis of mucopolysaccharides, stimulates hepatic synthesis of cholesterol and fatty acids, and is a cofactor in many enzymes, including arginase and alkaline phosphatase in the liver. (From AMA Drug Evaluations Annual 1992, p2035)
  • OXOGLURIC ACID 8 [hp_X]/mL - A family of compounds containing an oxo group with the general structure of 1,5-pentanedioic acid. (From Lehninger, Principles of Biochemistry, 1982, p442)
  • PHOSPHORUS 12 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
  • PORK LIVER 6 [hp_X]/mL
  • PYRUVIC ACID 8 [hp_X]/mL - An intermediate compound in the metabolism of carbohydrates, proteins, and fats. In thiamine deficiency, its oxidation is retarded and it accumulates in the tissues, especially in nervous structures. (From Stedman, 26th ed)
  • SODIUM DIETHYL OXALACETATE 12 [hp_X]/mL
  • SUCCINIC ACID 8 [hp_X]/mL - A water-soluble, colorless crystal with an acid taste that is used as a chemical intermediate, in medicine, the manufacture of lacquers, and to make perfume esters. It is also used in foods as a sequestrant, buffer, and a neutralizing agent. (Hawley's Condensed Chemical Dictionary, 12th ed, p1099; McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed, p1851)
  • SULFUR 12 [hp_X]/mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
  • SUS SCROFA GALLBLADDER 6 [hp_X]/mL
  • THYROID 6 [hp_X]/mL - A highly vascularized endocrine gland consisting of two lobes joined by a thin band of tissue with one lobe on each side of the TRACHEA. It secretes THYROID HORMONES from the follicular cells and CALCITONIN from the parafollicular cells thereby regulating METABOLISM and CALCIUM level in blood, respectively.

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are the Inactive Ingredients associated UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes of this product?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What is the Substance Name? An 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.
What kind of product is this? Indicates 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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product 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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
What is the NDC Exclude Flag? This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".