Metab Liquid
NDC 43742-1579

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1579?
  4. Metab Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Metab (ascorbicum acidum, cysteinum, manganese gluconate, alpha-ketoglutaricum acidum, fumaricum acidum, germanium sesquioxide, iodium, magnesium metallicum, natrum oxalaceticum, pulsatilla (pratensis), thyroidinum (suis), vanadium metallicum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc. This medication is typically used as a ascorbic acid [cs]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-1579 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43742-1579
Proprietary Name:
Metab
Non-Proprietary Name: [1]
Ascorbicum Acidum, Cysteinum, Manganese Gluconate, Alpha-ketoglutaricum Acidum, Fumaricum Acidum, Germanium Sesquioxide, Iodium, Magnesium Metallicum, Natrum Oxalaceticum, Pulsatilla (pratensis), Thyroidinum (suis), Vanadium Metallicum
Substance Name: [2]
Anemone Pratensis; Ascorbic Acid; Cysteine; Fumaric Acid; Germanium Sesquioxide; Iodine; Magnesium; Manganese Gluconate; Oxogluric Acid; Sodium Diethyl Oxalacetate; Sus Scrofa Thyroid; Vanadium
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]
Deseret Biologicals, Inc
Labeler Code:
43742
Product Label ID:
fbf89a37-dca2-4498-8866-234b033c5d42
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
10-07-2019
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43742-1579?

The NDC code 43742-1579 is assigned by the FDA to the product Metab. It is commonly known by its generic name, ascorbicum acidum, cysteinum, manganese gluconate, alpha-ketoglutaricum acidum, fumaricum acidum, germanium sesquioxide, iodium, magnesium metallicum, natrum oxalaceticum, pulsatilla (pratensis), thyroidinum (suis), vanadium metallicum. This pharmaceutical product is labeled by Deseret Biologicals, 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: 43742-1579-1. 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?

For the temporary relief of symptoms related to headache, joint pain, sweating, congestion, and fatigue.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the temporary relief of symptoms related to headache, joint pain, sweating, congestion, and fatigue.****These statements are based upon traditional homeopathic principles. 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.
  • ANEMONE PRATENSIS 12 [hp_X]/mL
  • ASCORBIC ACID 6 [hp_X]/mL - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
  • CYSTEINE 9 [hp_X]/mL - A thiol-containing non-essential amino acid that is oxidized to form CYSTINE.
  • FUMARIC ACID 12 [hp_X]/mL - see also record for ferrous fumarate; use FUMARATES for general fumaric acid esters
  • GERMANIUM SESQUIOXIDE 12 [hp_X]/mL
  • IODINE 12 [hp_X]/mL - A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
  • MAGNESIUM 12 [hp_X]/mL - A metallic element that has the atomic symbol Mg, atomic number 12, and atomic weight 24.31. It is important for the activity of many enzymes, especially those involved in OXIDATIVE PHOSPHORYLATION.
  • MANGANESE GLUCONATE 10 [hp_X]/mL
  • OXOGLURIC 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)
  • SODIUM DIETHYL OXALACETATE 12 [hp_X]/mL
  • SUS SCROFA THYROID 12 [hp_X]/mL
  • VANADIUM 12 [hp_X]/mL - A metallic element with the atomic symbol V, atomic number 23, and atomic weight 50.94. It is used in the manufacture of vanadium steel. Prolonged exposure can lead to chronic intoxication caused by absorption usually via the lungs.

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".