1. Home
  2. Labeler Index
  3. Deseret Biologicals, Inc.
  4. NDC Product Code: 43742-2095 Pollutox

NDC 43742-2095 Pollutox

Sulphuricum Acidum,Berberis Vulgaris,Arsenicum Album,Benzinum,Cadmium - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43742-2095?
  4. Pollutox Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
43742-2095
Proprietary Name:
Pollutox
Non-Proprietary Name: [1]
Sulphuricum Acidum, Berberis Vulgaris, Arsenicum Album, Benzinum, Cadmium Sulphuratum, Hydrofluoricum Acidum, Melatonin, Nitrogenum Oxygenatum, Nux Vomica, Petroleum, Plumbum Metallicum, Stannum Metallicum, Toluene, Acetone, Carbon Dioxide, Chlorinum, Mercurius Solubilis, Ozone, Uranium Nitricum
Substance Name: [2]
Acetone; Arsenic Trioxide; Benzene; Berberis Vulgaris Root Bark; Cadmium Sulfide; Carbon Dioxide; Chlorine; Hydrofluoric Acid; Kerosene; Lead; Melatonin; Mercurius Solubilis; Nitrous Oxide; Ozone; Strychnos Nux-vomica Seed; Sulfuric Acid; Tin; Toluene; Uranyl Nitrate Hexahydrate
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:
    e7000300-69ec-47db-8059-3f873d64f177
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    10-13-2023
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 43742-2095?

    The NDC code 43742-2095 is assigned by the FDA to the product Pollutox which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Pollutox is sulphuricum acidum, berberis vulgaris, arsenicum album, benzinum, cadmium sulphuratum, hydrofluoricum acidum, melatonin, nitrogenum oxygenatum, nux vomica, petroleum, plumbum metallicum, stannum metallicum, toluene, acetone, carbon dioxide, chlorinum, mercurius solubilis, ozone, uranium nitricum. 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 43742-2095-1 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 Pollutox?

    1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

    What are Pollutox 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.
    • ACETONE 12 [hp_X]/mL - A colorless liquid used as a solvent and an antiseptic. It is one of the ketone bodies produced during ketoacidosis.
    • ARSENIC TRIOXIDE 12 [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.
    • BENZENE 12 [hp_X]/mL - Toxic, volatile, flammable liquid hydrocarbon byproduct of coal distillation. It is used as an industrial solvent in paints, varnishes, lacquer thinners, gasoline, etc. Benzene causes central nervous system damage acutely and bone marrow damage chronically and is carcinogenic. It was formerly used as parasiticide.
    • BERBERIS VULGARIS ROOT BARK 8 [hp_X]/mL
    • CADMIUM SULFIDE 12 [hp_X]/mL
    • CARBON DIOXIDE 12 [hp_X]/mL - A colorless, odorless gas that can be formed by the body and is necessary for the respiration cycle of plants and animals.
    • CHLORINE 12 [hp_X]/mL - An element with atomic symbol Cl, atomic number 17, and atomic weight 35, and member of the halogen family.
    • HYDROFLUORIC ACID 12 [hp_X]/mL - Hydrofluoric acid. A solution of hydrogen fluoride in water. It is a colorless fuming liquid which can cause painful burns.
    • 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.
    • MELATONIN 12 [hp_X]/mL - A biogenic amine that is found in animals and plants. In mammals, melatonin is produced by the PINEAL GLAND. Its secretion increases in darkness and decreases during exposure to light. Melatonin is implicated in the regulation of SLEEP, mood, and REPRODUCTION. Melatonin is also an effective antioxidant.
    • MERCURIUS SOLUBILIS 12 [hp_X]/mL
    • NITROUS OXIDE 12 [hp_X]/mL - Nitrogen oxide (N2O). A colorless, odorless gas that is used as an anesthetic and analgesic. High concentrations cause a narcotic effect and may replace oxygen, causing death by asphyxia. It is also used as a food aerosol in the preparation of whipping cream.
    • OZONE 16 [hp_X]/mL - The unstable triatomic form of oxygen, O3. It is a powerful oxidant that is produced for various chemical and industrial uses. Its production is also catalyzed in the ATMOSPHERE by ULTRAVIOLET RAY irradiation of oxygen or other ozone precursors such as VOLATILE ORGANIC COMPOUNDS and NITROGEN OXIDES. About 90% of the ozone in the atmosphere exists in the stratosphere (STRATOSPHERIC OZONE).
    • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
    • SULFURIC ACID 6 [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.
    • TOLUENE 12 [hp_X]/mL - A widely used industrial solvent.
    • URANYL NITRATE HEXAHYDRATE 15 [hp_C]/mL

    Which are Pollutox UNII Codes?

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

    Which are Pollutox 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.

    [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".