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  4. NDC Product Code: 43857-0249 Diathesis I

NDC 43857-0249 Diathesis I

Manganum Metallicum,Germanium Sesquioxide,Fel Tauri,Hepar Suis,Ginkgo - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43857-0249?
  4. Diathesis I Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
43857-0249
Proprietary Name:
Diathesis I
Non-Proprietary Name: [1]
Manganum Metallicum, Germanium Sesquioxide, Fel Tauri, Hepar Suis, Ginkgo Biloba, Cysteinum, Manganese Gluconate, Alpha-ketoglutaricum Acidum, Arsenicum Album, Fumaricum Acidum, Phosphorus, Sodium Oxalate, Sulphur
Substance Name: [2]
.alpha.-ketoglutaric Acid; Arsenic Trioxide; Bos Taurus Bile; Cysteine; Fumaric Acid; Germanium Sesquioxide; Ginkgo; Manganese; Manganese Gluconate; Phosphorus; Pork Liver; Sodium Oxalate; Sulfur
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]
    Bioactive Nutritionals, Inc.
    Labeler Code:
    43857
    Product Label ID:
    e8c3b763-7d54-48b1-8db8-a5b47ce7aeeb
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    01-09-2014
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

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    Product Details

    What is NDC 43857-0249?

    The NDC code 43857-0249 is assigned by the FDA to the product Diathesis I which is a human over the counter drug product labeled by Bioactive Nutritionals, Inc.. The generic name of Diathesis I is manganum metallicum, germanium sesquioxide, fel tauri, hepar suis, ginkgo biloba, cysteinum, manganese gluconate, alpha-ketoglutaricum acidum, arsenicum album, fumaricum acidum, phosphorus, sodium oxalate, sulphur. 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 43857-0249-1 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 Diathesis I?

    For temporary relief of inflammation of bones or joints, with nightly digging pains, general soreness and aching soreness over entire body when touched, and burning in soles and hands at night. For temporary relief of inflammation of bones or joints, with nightly digging pains, general soreness and aching soreness over entire body when touched, and burning in soles and hands at night.

    What are Diathesis I 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.
    • .ALPHA.-KETOGLUTARIC ACID 12 [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)
    • ARSENIC TRIOXIDE 12 [hp_X]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
    • BOS TAURUS BILE 6 [hp_X]/mL
    • CYSTEINE 9 [hp_X]/mL - A thiol-containing non-essential amino acid that is oxidized to form CYSTINE.
    • FUMARIC ACID 12 [hp_X]/mL
    • GERMANIUM SESQUIOXIDE 8 [hp_X]/mL
    • GINKGO 6 [hp_X]/mL
    • MANGANESE 9 [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)
    • MANGANESE GLUCONATE 10 [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.
    • PORK LIVER 6 [hp_X]/mL
    • SODIUM OXALATE 12 [hp_X]/mL - A strong dicarboxylic acid occurring in many plants and vegetables. It is produced in the body by metabolism of glyoxylic acid or ascorbic acid. It is not metabolized but excreted in the urine. It is used as an analytical reagent and general reducing agent.
    • 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.

    Which are Diathesis I UNII Codes?

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

    Which are Diathesis I 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 Diathesis I?

    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.

    * Please review the disclaimer below.

    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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".