NDC 43857-0593 Dentox

Berberis Vulgaris,Glycyrrhiza Glabra,Lappa Major,Stillingia Sylvatica,Trifolium - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
43857-0593
Proprietary Name:
Dentox
Non-Proprietary Name: [1]
Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Trifolium Pratense, Phytolacca Decandra, Lymph Node(suis), Medulla Ossis Suis, Thymus (suis), Thyroidinum (suis), Calcarea Fluorica, Natrum Fluoratum, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Eugenol, Formalinum, Lidocaine, Mercurius Solubilis, Molybdenum, Niccolum Metallicum, Palladium Metallicum, Stannum Metallicum, Titanium Metallicum, Zincum Metallicum
Substance Name: [2]
Arctium Lappa Root; Berberis Vulgaris Root Bark; Calcium Fluoride; Copper; Eugenol; Formaldehyde Solution; Glycyrrhiza Glabra; Gold; Lidocaine; Mercurius Solubilis; Molybdenum; Nickel; Palladium; Phytolacca Americana Root; Silver; Sodium Fluoride; Stillingia Sylvatica Root; Sus Scrofa Bone Marrow; Sus Scrofa Lymph; Sus Scrofa Thymus; Thyroid, Porcine; Tin; Titanium; Trifolium Pratense Flower; Zinc
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 Nutritional, Inc.
    Labeler Code:
    43857
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    02-14-2023
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 43857-0593-1

    Package Description: 30 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 43857-0593?

    The NDC code 43857-0593 is assigned by the FDA to the product Dentox which is a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Dentox is berberis vulgaris, glycyrrhiza glabra, lappa major, stillingia sylvatica, trifolium pratense, phytolacca decandra, lymph node(suis), medulla ossis suis, thymus (suis), thyroidinum (suis), calcarea fluorica, natrum fluoratum, argentum metallicum, aurum metallicum, cuprum metallicum, eugenol, formalinum, lidocaine, mercurius solubilis, molybdenum, niccolum metallicum, palladium metallicum, stannum metallicum, titanium metallicum, zincum metallicum. 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 43857-0593-1 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 Dentox?

    10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

    What are Dentox 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.
    • ARCTIUM LAPPA ROOT 3 [hp_X]/mL
    • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
    • CALCIUM FLUORIDE 12 [hp_X]/mL - Calcium fluoride. Occurring in nature as the mineral fluorite or fluorspar. It is the primary source of fluorine and its compounds. Pure calcium fluoride is used as a catalyst in dehydration and dehydrogenation and is used to fluoridate drinking water. (From Merck Index, 11th ed)
    • COPPER 12 [hp_X]/mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
    • EUGENOL 12 [hp_X]/mL - A cinnamate derivative of the shikimate pathway found in CLOVE OIL and other PLANTS.
    • FORMALDEHYDE SOLUTION 12 [hp_X]/mL
    • GLYCYRRHIZA GLABRA 3 [hp_X]/mL - A genus of leguminous herbs or shrubs whose roots yield GLYCYRRHETINIC ACID and its derivative, CARBENOXOLONE.
    • GOLD 12 [hp_X]/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.
    • LIDOCAINE 12 [hp_X]/mL - A local anesthetic and cardiac depressant used as an antiarrhythmia agent. Its actions are more intense and its effects more prolonged than those of PROCAINE but its duration of action is shorter than that of BUPIVACAINE or PRILOCAINE.
    • MERCURIUS SOLUBILIS 12 [hp_X]/mL
    • MOLYBDENUM 12 [hp_X]/mL - A metallic element with the atomic symbol Mo, atomic number 42, and atomic weight 95.95. It is an essential trace element, being a component of the enzymes xanthine oxidase, aldehyde oxidase, and nitrate reductase.
    • NICKEL 12 [hp_X]/mL - A trace element with the atomic symbol Ni, atomic number 28, and atomic weight 58.69. It is a cofactor of the enzyme UREASE.
    • PALLADIUM 12 [hp_X]/mL - A chemical element having an atomic weight of 106.4, atomic number of 46, and the symbol Pd. It is a white, ductile metal resembling platinum, and following it in abundance and importance of applications. It is used in dentistry in the form of gold, silver, and copper alloys.
    • PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
    • SILVER 12 [hp_X]/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.
    • SODIUM FLUORIDE 12 [hp_X]/mL - A source of inorganic fluoride which is used topically to prevent dental caries.
    • STILLINGIA SYLVATICA ROOT 3 [hp_X]/mL
    • SUS SCROFA BONE MARROW 8 [hp_X]/mL
    • SUS SCROFA LYMPH 8 [hp_X]/mL
    • SUS SCROFA THYMUS 8 [hp_X]/mL
    • THYROID, PORCINE 8 [hp_X]/mL
    • TIN 12 [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.
    • TITANIUM 12 [hp_X]/mL - A dark-gray, metallic element of widespread distribution but occurring in small amounts with atomic number, 22, atomic weight, 47.867 and symbol, Ti; specific gravity, 4.5; used for fixation of fractures.
    • TRIFOLIUM PRATENSE FLOWER 3 [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.

    Which are Dentox UNII Codes?

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

    Which are Dentox 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 Dentox?

    * 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".