NDC 83027-0120 Enviro Detox Formula

Lappa Major,Taraxacum Officinale,Trifolium Pratense,Spinacia,Petroleum,Plumbum - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
Proprietary Name:
Enviro Detox Formula
Non-Proprietary Name: [1]
Lappa Major, Taraxacum Officinale, Trifolium Pratense, Spinacia, Petroleum, Plumbum Metallicum, Sulphuricum Acidum, Ammonium Phosphoricum, Arsenicum Album, Chromium (metallicum), Cuprum Metallicum, Dibromoethane, Kreosotum, Mercurius Vivus, Mtbe (tert-butyl Methyl Ether), Nitricum Acidum, Radium Bromatum
Substance Name: [2]
Ammonium Phosphate, Dibasic; Arctium Lappa Root; Arsenic Trioxide; Chromium; Copper; Ethylene Dibromide; Kerosene; Lead; Mercury; Nitric Acid; Radium Bromide; Spinacia Oleracea Root; Sulfuric Acid; Taraxacum Officinale; Tert-butyl Methyl Ether; Trifolium Pratense Flower; Wood Creosote
NDC Directory Status:
Human Otc Drug
Product Type: [3]
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Code:
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    Listing Expiration Date: [11]
    Exclude Flag: [12]
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    Product Details

    What is NDC 83027-0120?

    The NDC code 83027-0120 is assigned by the FDA to the product Enviro Detox Formula which is a human over the counter drug product labeled by Nutritional Specialties, Inc.. The generic name of Enviro Detox Formula is lappa major, taraxacum officinale, trifolium pratense, spinacia, petroleum, plumbum metallicum, sulphuricum acidum, ammonium phosphoricum, arsenicum album, chromium (metallicum), cuprum metallicum, dibromoethane, kreosotum, mercurius vivus, mtbe (tert-butyl methyl ether), nitricum acidum, radium bromatum. The product's dosage form is spray and is administered via oral form. The product is distributed in a single package with assigned NDC code 83027-0120-1 60 ml in 1 bottle, spray . 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 Enviro Detox Formula?

    Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.

    What are Enviro Detox Formula 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
    • ARSENIC TRIOXIDE 30 [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.
    • CHROMIUM 30 [hp_X]/mL - A trace element that plays a role in glucose metabolism. It has the atomic symbol Cr, atomic number 24, and atomic weight 52. According to the Fourth Annual Report on Carcinogens (NTP85-002,1985), chromium and some of its compounds have been listed as known carcinogens.
    • COPPER 30 [hp_X]/mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
    • ETHYLENE DIBROMIDE 30 [hp_X]/mL - An effective soil fumigant, insecticide, and nematocide. In humans, it causes severe burning of skin and irritation of the eyes and respiratory tract. Prolonged inhalation may cause liver necrosis. It is also used in gasoline. Members of this group have caused liver and lung cancers in rodents. According to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985), 1,2-dibromoethane may reasonably be anticipated to be a carcinogen.
    • KEROSENE 12 [hp_X]/mL - A refined petroleum fraction used as a fuel as well as a solvent.
    • LEAD 12 [hp_X]/mL - A soft, grayish metal with poisonous salts; atomic number 82, atomic weight 207.2, symbol Pb.
    • MERCURY 30 [hp_X]/mL - A silver metallic element that exists as a liquid at room temperature. It has the atomic symbol Hg (from hydrargyrum, liquid silver), atomic number 80, and atomic weight 200.59. Mercury is used in many industrial applications and its salts have been employed therapeutically as purgatives, antisyphilitics, disinfectants, and astringents. It can be absorbed through the skin and mucous membranes which leads to MERCURY POISONING. Because of its toxicity, the clinical use of mercury and mercurials is diminishing.
    • NITRIC ACID 30 [hp_X]/mL - Nitric acid (HNO3). A colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals. Continued exposure to vapor may cause chronic bronchitis; chemical pneumonitis may occur. (From Merck Index, 11th ed)
    • RADIUM BROMIDE 30 [hp_X]/mL
    • SULFURIC ACID 12 [hp_X]/mL
    • TARAXACUM OFFICINALE 3 [hp_X]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
    • WOOD CREOSOTE 30 [hp_X]/mL

    Which are Enviro Detox Formula UNII Codes?

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

    Which are Enviro Detox Formula 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:

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    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".