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  4. NDC Product Code: 43742-1280 Detox Iii

NDC 43742-1280 Detox Iii

Dulcamara,Echinacea (angustifolia),Aesculus Hippocastanum,Antimonium Tartaricum,Ascorbic - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1280?
  4. Detox Iii Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
43742-1280
Proprietary Name:
Detox Iii
Non-Proprietary Name: [1]
Dulcamara, Echinacea (angustifolia), Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbic Acid, Coccus Cacti, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Pulsatilla (vulgaris), Sarcolacticum Acidum, Conium Maculatum, Lymph Node (suis), Sulphur, Glandula Suprarenalis Suis, L-phenylalanine, Calcarea Phosphorica, Ferrum Phosphoricum, Hepar Suis, Hypothalamus Suis, Spleen (suis), Cortisone Aceticum, Mercurius Solubilis, Baryta Carbonica, Glyphosate, Funiculus Umbilicalis Suis
Substance Name: [2]
Antimony Potassium Tartrate; Ascorbic Acid; Barium Carbonate; Bisphenol A; Bromine; Chlorine; Conium Maculatum Flowering Top; Cortisone Acetate; Echinacea Angustifolia; Escherichia Coli; Ferrum Phosphoricum; Galium Aparine; Gentiana Lutea Root; Geranium Robertianum; Glyphosate; Horse Chestnut; Hydrofluoric Acid; Iodine; Lactic Acid, L-; Liothyronine; Mercurius Solubilis; Phenylalanine; Pork Liver; Protortonia Cacti; Pulsatilla Vulgaris Whole; Salmonella Enterica Subsp. Enterica Serovar Enteritidis; Solanum Dulcamara Top; Sulfur; Sus Scrofa Adrenal Gland; Sus Scrofa Bone Marrow; Sus Scrofa Hypothalamus; Sus Scrofa Lymph; Sus Scrofa Spleen; Sus Scrofa Tonsil; Sus Scrofa Umbilical Cord; Tribasic Calcium Phosphate
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]
    Deseret Biologicals, Inc.
    Labeler Code:
    43742
    Product Label ID:
    6eb6eb26-c690-473c-a5cb-cb65613d7b96
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    10-31-2018
    End Marketing Date: [10]
    06-16-2025
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 43742-1280?

    The NDC code 43742-1280 is assigned by the FDA to the product Detox Iii which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Detox Iii is dulcamara, echinacea (angustifolia), aesculus hippocastanum, antimonium tartaricum, ascorbic acid, coccus cacti, galium aparine, gentiana lutea, geranium robertianum, pulsatilla (vulgaris), sarcolacticum acidum, conium maculatum, lymph node (suis), sulphur, glandula suprarenalis suis, l-phenylalanine, calcarea phosphorica, ferrum phosphoricum, hepar suis, hypothalamus suis, spleen (suis), cortisone aceticum, mercurius solubilis, baryta carbonica, glyphosate, funiculus umbilicalis suis. 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 43742-1280-1 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 Detox Iii?

    For temporary relief of symptoms related to improper breakdown and excretion of allergenic substances, including pain, fatigue, cramping and upper respiratory allergy.****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 improper breakdown and excretion of allergenic substances, including pain, fatigue, cramping and upper respiratory allergy.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

    What are Detox Iii 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.

    Which are Detox Iii UNII Codes?

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

    Which are Detox Iii 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:

    * 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.

    [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".