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NDC 44911-0439 Lungex II

Ginkgo Biloba,Colon (suis),Lung (suis),Pancreas Suis,Germanium Sesquioxide,Cuprum - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0439?
  4. Lungex II Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 44911-0439 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
44911-0439
Proprietary Name:
Lungex II
Non-Proprietary Name: [1]
Ginkgo Biloba, Colon (suis), Lung (suis), Pancreas Suis, Germanium Sesquioxide, Cuprum Metallicum, Manganum Metallicum, Stannum Metallicum, Alpha-ketoglutaricum Acidum, Citricum Acidum, Fumaricum Acidum, Malic Acid, Pyruvic Acid, Succinicum Acidum, Naphthoquinone, Arsenicum Metallicum, Calcarea Carbonica, Aconiticum Acidum, Cis, Natrum Oxalaceticum, Phosphorus
Substance Name: [2]
1,2-naphthoquinone; Aconitic Acid; Arsenic; Citric Acid Monohydrate; Copper; Fumaric Acid; Germanium Sesquioxide; Ginkgo; Malic Acid; Manganese; Oxogluric Acid; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Pyruvic Acid; Sodium Diethyl Oxalacetate; Succinic Acid; Sus Scrofa Colon; Sus Scrofa Lung; Sus Scrofa Pancreas; Tin
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
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 Name: [5]
Energique, Inc.
Labeler Code:
44911
Product Label ID:
ddf7fc46-95b7-44b4-b7ca-96a066a3fa2b
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
09-08-2017
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 44911-0439?

The NDC code 44911-0439 is assigned by the FDA to the product Lungex II which is a human over the counter drug product labeled by Energique, Inc.. The generic name of Lungex II is ginkgo biloba, colon (suis), lung (suis), pancreas suis, germanium sesquioxide, cuprum metallicum, manganum metallicum, stannum metallicum, alpha-ketoglutaricum acidum, citricum acidum, fumaricum acidum, malic acid, pyruvic acid, succinicum acidum, naphthoquinone, arsenicum metallicum, calcarea carbonica, aconiticum acidum, cis, natrum oxalaceticum, phosphorus. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 44911-0439-1 30 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Lungex II?

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

What are Lungex II Active Ingredients?

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.
  • 1,2-NAPHTHOQUINONE 9 [hp_X]/mL
  • ACONITIC ACID 12 [hp_X]/mL - A tricarboxylic acid with the formula (COOH)-CH2-C(COOH)=CH-COOH.
  • 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)
  • CITRIC ACID MONOHYDRATE 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.
  • COPPER 8 [hp_X]/mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
  • FUMARIC ACID 8 [hp_X]/mL
  • 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.
  • 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)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
  • 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.
  • 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)
  • SUS SCROFA COLON 6 [hp_X]/mL
  • SUS SCROFA LUNG 6 [hp_X]/mL
  • SUS SCROFA PANCREAS 6 [hp_X]/mL
  • TIN 8 [hp_X]/mL - A trace element that is required in bone formation. It has the atomic symbol Sn, atomic number 50, and atomic weight 118.71.

Which are Lungex II UNII Codes?

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

Which are Lungex II Inactive Ingredients 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 for Lungex II?

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Product Footnotes

[1] 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.

[2] 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.

[3] 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".