NDC 72198-0003 Metabolic Detox

Beta Vulgaris,Boldo,Chelidonium Majus,Sarsaparilla (smilax Regelii),Gelsemium - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
72198-0003
Proprietary Name:
Metabolic Detox
Non-Proprietary Name: [1]
Beta Vulgaris, Boldo, Chelidonium Majus, Sarsaparilla (smilax Regelii), Gelsemium Sempervirens, Veratrum Album, Ferrum Metallicum, Iodium, Lycopodium Clavatum, Nux Vomica, Pulsatilla (vulgaris), Selenium Metallicum, Thuja Occidentalis, Zincum Metallicum
Substance Name: [2]
Beta Vulgaris; Chelidonium Majus; Gelsemium Sempervirens Root; Iodine; Iron; Lycopodium Clavatum Spore; Peumus Boldus Leaf; Pulsatilla Vulgaris; Sarsaparilla; Selenium; Strychnos Nux-vomica Seed; Thuja Occidentalis Leafy Twig; Veratrum Album Root; 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]
    Healthsource Of New England Llc
    Labeler Code:
    72198
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    10-18-2018
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 72198-0003-1

    Package Description: 30 mL in 1 PACKAGE

    Product Details

    What is NDC 72198-0003?

    The NDC code 72198-0003 is assigned by the FDA to the product Metabolic Detox which is a human over the counter drug product labeled by Healthsource Of New England Llc. The generic name of Metabolic Detox is beta vulgaris, boldo, chelidonium majus, sarsaparilla (smilax regelii), gelsemium sempervirens, veratrum album, ferrum metallicum, iodium, lycopodium clavatum, nux vomica, pulsatilla (vulgaris), selenium metallicum, thuja occidentalis, 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 72198-0003-1 30 ml in 1 package . 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 Metabolic Detox?

    For temporary relief of symptoms related to excretory dysfunction including mucous congestion.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to excretory dysfunction including mucous congestion.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

    What are Metabolic Detox 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.
    • BETA VULGARIS 3 [hp_X]/mL - A species of the Beta genus. Cultivars are used as a source of beets (root) or chard (leaves).
    • CHELIDONIUM MAJUS 3 [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).
    • GELSEMIUM SEMPERVIRENS ROOT 8 [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.
    • IRON 12 [hp_X]/mL - A metallic element with atomic symbol Fe, atomic number 26, and atomic weight 55.85. It is an essential constituent of HEMOGLOBINS; CYTOCHROMES; and IRON-BINDING PROTEINS. It plays a role in cellular redox reactions and in the transport of OXYGEN.
    • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
    • PEUMUS BOLDUS LEAF 3 [hp_X]/mL
    • PULSATILLA VULGARIS 12 [hp_X]/mL
    • SARSAPARILLA 6 [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.
    • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
    • THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL
    • VERATRUM ALBUM ROOT 8 [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 Metabolic Detox UNII Codes?

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

    Which are Metabolic Detox 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 Metabolic Detox?

    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".