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  4. NDC Product Code: 43742-1207 Boldo, Chelidonium Majus, Taraxacum Officinale, Arsenicum Album, Beta Vulgaris, Cobaltum Metallicum, Cuprum Metallicum, Iodium, Lycopodium Clavatum, Petroselinum Sativum, Phosphoricum Acidum, Selenium Metallicum, Zincum Metallicum, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methyl Paraben, Propyl Paraben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum

NDC 43742-1207 Boldo, Chelidonium Majus, Taraxacum Officinale, Arsenicum Album, Beta Vulgaris, Cobaltum Metallicum, Cuprum Metallicum, Iodium, Lycopodium Clavatum, Petroselinum Sativum, Phosphoricum Acidum, Selenium Metallicum, Zincum Metallicum, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methyl Paraben, Propyl Paraben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum

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

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1207?
  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:
43742-1207
Proprietary Name:
Boldo, Chelidonium Majus, Taraxacum Officinale, Arsenicum Album, Beta Vulgaris, Cobaltum Metallicum, Cuprum Metallicum, Iodium, Lycopodium Clavatum, Petroselinum Sativum, Phosphoricum Acidum, Selenium Metallicum, Zincum Metallicum, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methyl Paraben, Propyl Paraben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum
Non-Proprietary Name: [1]
Boldo, Chelidonium Majus, Taraxacum Officinale, Arsenicum Album, Beta Vulgaris, Cobaltum Metallicum, Cuprum Metallicum, Iodium, Lycopodium Clavatum, Petroselinum Sativum, Phosphoricum Acidum, Selenium Metallicum, Zincum Metallicum, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methyl Paraben, Propyl Paraben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum
Substance Name: [2]
Arsenic Trioxide; Aspartame; Benzalkonium Chloride; Beta Vulgaris; Chelidonium Majus; Cobalt; Copper; Formaldehyde; Iodine; Lycopodium Clavatum Spore; Methylene Chloride; Methylparaben; Petroselinum Crispum; Peumus Boldus Leaf; Phosphoric Acid; Propylparaben; Selenium; Sodium Benzoate; Sodium Citrate; Taraxacum Officinale; Titanium Dioxide; Zinc; Zinc Oxide
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]
04-12-2018
End Marketing Date: [10]
08-19-2025
Exclude Flag: [12]
N
Unfinished Product: [13]
Yes
Code Navigator:

Code Structure Chart

Product Details

What is NDC 43742-1207?

The NDC code 43742-1207 is assigned by the FDA to the UNFINISHED product Boldo, Chelidonium Majus, Taraxacum Officinale, Arsenicum Album, Beta Vulgaris, Cobaltum Metallicum, Cuprum Metallicum, Iodium, Lycopodium Clavatum, Petroselinum Sativum, Phosphoricum Acidum, Selenium Metallicum, Zincum Metallicum, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methyl Paraben, Propyl Paraben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum which is drug for further processing product labeled by Deseret Biologicals, Inc.. The generic name of Boldo, Chelidonium Majus, Taraxacum Officinale, Arsenicum Album, Beta Vulgaris, Cobaltum Metallicum, Cuprum Metallicum, Iodium, Lycopodium Clavatum, Petroselinum Sativum, Phosphoricum Acidum, Selenium Metallicum, Zincum Metallicum, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methyl Paraben, Propyl Paraben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum is boldo, chelidonium majus, taraxacum officinale, arsenicum album, beta vulgaris, cobaltum metallicum, cuprum metallicum, iodium, lycopodium clavatum, petroselinum sativum, phosphoricum acidum, selenium metallicum, zincum metallicum, aspartame, benzalkonium chloride, formalinum, methylene chloride, methyl paraben, propyl paraben, sodium benzoate, sodium citrate, titanium dioxide, zincum oxydatum. The product's dosage form is liquid. The product is distributed in a single package with assigned NDC code 43742-1207-1 960 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 Boldo, Chelidonium Majus, Taraxacum Officinale, Arsenicum Album, Beta Vulgaris, Cobaltum Metallicum, Cuprum Metallicum, Iodium, Lycopodium Clavatum, Petroselinum Sativum, Phosphoricum Acidum, Selenium Metallicum, Zincum Metallicum, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methyl Paraben, Propyl Paraben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum 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.
  • 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.
  • ASPARTAME 30 [hp_X]/mL - Flavoring agent sweeter than sugar, metabolized as PHENYLALANINE and ASPARTIC ACID.
  • BENZALKONIUM CHLORIDE 30 [hp_X]/mL
  • BETA VULGARIS 12 [hp_X]/mL - A species of the Beta genus. Cultivars are used as a source of beets (root) or chard (leaves).
  • CHELIDONIUM MAJUS 6 [hp_X]/mL - A plant species of the family PAPAVERACEAE. The common name greater celandine is similar to lesser celandine (Ficaria verna), and celandine poppy (Stylophorum diphyllum). It has been used in folk medicine and its latex contains biologically active compounds including BENZOPHENANTHRIDINES alkaloids (e.g., Chelerythrine).
  • COBALT 12 [hp_X]/mL - A trace element that is a component of vitamin B12. It has the atomic symbol Co, atomic number 27, and atomic weight 58.93. It is used in nuclear weapons, alloys, and pigments. Deficiency in animals leads to anemia; its excess in humans can lead to erythrocytosis.
  • COPPER 12 [hp_X]/mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
  • FORMALDEHYDE 30 [hp_X]/mL - A highly reactive aldehyde gas formed by oxidation or incomplete combustion of hydrocarbons. In solution, it has a wide range of uses: in the manufacture of resins and textiles, as a disinfectant, and as a laboratory fixative or preservative. Formaldehyde solution (formalin) is considered a hazardous compound, and its vapor toxic. (From Reynolds, Martindale The Extra Pharmacopoeia, 30th ed, p717)
  • 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.
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • METHYLENE CHLORIDE 30 [hp_X]/mL - A chlorinated hydrocarbon that has been used as an inhalation anesthetic and acts as a narcotic in high concentrations. Its primary use is as a solvent in manufacturing and food technology.
  • METHYLPARABEN 30 [hp_X]/mL
  • PETROSELINUM CRISPUM 12 [hp_X]/mL - A plant genus of the family APIACEAE used for flavoring food.
  • PEUMUS BOLDUS LEAF 6 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • PROPYLPARABEN 30 [hp_X]/mL
  • SELENIUM 12 [hp_X]/mL - An element with the atomic symbol Se, atomic number 34, and atomic weight 78.97. It is an essential micronutrient for mammals and other animals but is toxic in large amounts. Selenium protects intracellular structures against oxidative damage. It is an essential component of GLUTATHIONE PEROXIDASE.
  • SODIUM BENZOATE 30 [hp_X]/mL - The sodium salt of BENZOIC ACID. It is used as an antifungal preservative in pharmaceutical preparations and foods. It may also be used as a test for liver function.
  • SODIUM CITRATE 30 [hp_X]/mL - Sodium salts of citric acid that are used as buffers and food preservatives. They are used medically as anticoagulants in stored blood, and for urine alkalization in the prevention of KIDNEY STONES.
  • TARAXACUM OFFICINALE 6 [hp_X]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
  • TITANIUM DIOXIDE 30 [hp_X]/mL
  • ZINC 12 [hp_X]/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.
  • ZINC OXIDE 30 [hp_X]/mL - A mild astringent and topical protectant with some antiseptic action. It is also used in bandages, pastes, ointments, dental cements, and as a sunblock.

* 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.

[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.