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  4. NDC Product Code: 43742-1576 Aqua Sulis, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Lapis Albus, Manganum Metallicum, Vanadium Metallicum, Viscum Album, Zincum Metallicum

NDC 43742-1576 Aqua Sulis, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Lapis Albus, Manganum Metallicum, Vanadium Metallicum, Viscum Album, Zincum Metallicum

Liquid - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1576?
  4. Active Ingredients

Product Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.
NDC Product Code:
43742-1576
Proprietary Name:
Aqua Sulis, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Lapis Albus, Manganum Metallicum, Vanadium Metallicum, Viscum Album, Zincum Metallicum
Non-Proprietary Name: [1]
Aqua Sulis, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Lapis Albus, Manganum Metallicum, Vanadium Metallicum, Viscum Album, Zincum Metallicum
Substance Name: [2]
Calcium Hexafluorosilicate; Copper; Gold; Manganese; Silver; Vanadium; Viscum Album Fruiting Top; Water; Zinc
NDC Directory Status:
Drug For Further Processing
Product Type: [3]
UNFINISHED 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.
Labeler Name: [5]
Deseret Biologicals, Inc.
Labeler Code:
43742
Marketing Category: [8]
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date: [9]
10-01-2019
End Marketing Date: [10]
01-15-2025
Exclude Flag: [12]
N
Unfinished Product: [13]
Yes
Code Navigator:

Code Structure Chart

Product Details

What is NDC 43742-1576?

The NDC code 43742-1576 is assigned by the FDA to the UNFINISHED product Aqua Sulis, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Lapis Albus, Manganum Metallicum, Vanadium Metallicum, Viscum Album, Zincum Metallicum which is drug for further processing product labeled by Deseret Biologicals, Inc.. The generic name of Aqua Sulis, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Lapis Albus, Manganum Metallicum, Vanadium Metallicum, Viscum Album, Zincum Metallicum is aqua sulis, argentum metallicum, aurum metallicum, cuprum metallicum, lapis albus, manganum metallicum, vanadium metallicum, viscum album, zincum metallicum. The product's dosage form is liquid. The product is distributed in a single package with assigned NDC code 43742-1576-1 960 ml in 1 bottle, plastic . 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 Aqua Sulis, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Lapis Albus, Manganum Metallicum, Vanadium Metallicum, Viscum Album, Zincum Metallicum 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.
  • CALCIUM HEXAFLUOROSILICATE 1 [hp_M]/mL
  • COPPER 1 [hp_M]/mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
  • GOLD 1 [hp_M]/mL - A yellow metallic element with the atomic symbol Au, atomic number 79, and atomic weight 197. It is used in jewelry, goldplating of other metals, as currency, and in dental restoration. Many of its clinical applications, such as ANTIRHEUMATIC AGENTS, are in the form of its salts.
  • MANGANESE 1 [hp_M]/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)
  • SILVER 1 [hp_M]/mL - An element with the atomic symbol Ag, atomic number 47, and atomic weight 107.87. It is a soft metal that is used medically in surgical instruments, dental prostheses, and alloys. Long-continued use of silver salts can lead to a form of poisoning known as ARGYRIA.
  • VANADIUM 1 [hp_M]/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.
  • VISCUM ALBUM FRUITING TOP 1 [hp_M]/mL
  • WATER 30 [hp_C]/mL - A clear, odorless, tasteless liquid that is essential for most animal and plant life and is an excellent solvent for many substances. The chemical formula is hydrogen oxide (H2O). (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
  • ZINC 1 [hp_M]/mL - A metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.

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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.

[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.

[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

[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".

[13] What is an Unfinished Product? - This field indicates if the product is an unfinished drug. An unfinished drug is an active pharmaceutical ingredient either alone or with other ingredients that is not a finished drug product. Unfinished drugs are used to process other drugs or for drug compounding.