NDC 55758-318 Desintox

Antimonium Crudum, Argentum Nitricum, Cholesterinum,Robinia Pseudo-acacia, Carbo - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
55758-318
Proprietary Name:
Desintox
Non-Proprietary Name: [1]
Antimonium Crudum, Argentum Nitricum, Cholesterinum, Robinia Pseudo-acacia, Carbo Vegetabilis, Cinchona, Aesculus Hippocastanum, Arnica Montana, Berberis Vulgaris, Ceanothus Americanus, Cynara Scolymus, Equisetum Arvense, Erigeron Canadensis, Fucus Vesiculosus, Ginkgo Biloba, Hamamelis Virginiana, Helonias Dioica, Hydrastis Canadensis, Hydrastis Canadensis, Lappa Major, Lespedeza Capitata, Raphanus Sativus, Taraxacum Officinale, Viburnum Prunifolium, Vitis Vinifera, Ranunculus Bulbosus
Substance Name: [2]
Activated Charcoal; Antimony Trisulfide; Arctium Lappa Root; Arnica Montana; Berberis Vulgaris Root Bark; Ceanothus Americanus Leaf; Chamaelirium Luteum Root; Cinchona Bark; Cynara Scolymus Leaf; Equisetum Arvense Top; Erigeron Canadensis; Fucus Vesiculosus; Ginkgo; Goldenseal; Hamamelis Virginiana Root Bark/stem Bark; Horse Chestnut; Lespedeza Capitata Flowering Top; Radish; Ranunculus Bulbosus; Robinia Pseudoacacia Bark; Silver Nitrate; Taraxacum Officinale; Viburnum Prunifolium Bark; Vitis Vinifera Whole
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]
    Pharmadel Llc
    Labeler Code:
    55758
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    01-01-2019
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 55758-318-02

    Package Description: 1 BOTTLE in 1 BOX / 60 mL in 1 BOTTLE

    Product Details

    What is NDC 55758-318?

    The NDC code 55758-318 is assigned by the FDA to the product Desintox which is a human over the counter drug product labeled by Pharmadel Llc. The generic name of Desintox is antimonium crudum, argentum nitricum, cholesterinum, robinia pseudo-acacia, carbo vegetabilis, cinchona, aesculus hippocastanum, arnica montana, berberis vulgaris, ceanothus americanus, cynara scolymus, equisetum arvense, erigeron canadensis, fucus vesiculosus, ginkgo biloba, hamamelis virginiana, helonias dioica, hydrastis canadensis, hydrastis canadensis, lappa major, lespedeza capitata, raphanus sativus, taraxacum officinale, viburnum prunifolium, vitis vinifera, ranunculus bulbosus. 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 55758-318-02 1 bottle in 1 box / 60 ml in 1 bottle. 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 Desintox?

    Shake well before each useadults and children over 12 years of age: place 20 drops in a small glass of water two (2) times a day, 15 minutes before a mealallow medicine to remain in the mouth for 15 seconds before swallowing

    What are Desintox 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 Desintox UNII Codes?

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

    Which are Desintox 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 Desintox?

    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".