Pollutox Liquid
NDC 43742-2037

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43742-2037?
  4. Pollutox Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Pollutox (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, uranium nitricum, ozone) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc.. This medication is typically used as a allergens [cs]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-2037 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43742-2037
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, Uranium Nitricum, Ozone
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
Code Navigator:

Clinical Specifications

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 & Regulatory Data

Labeler Name: [5]
Deseret Biologicals, Inc.
Labeler Code:
43742
Product Label ID:
14a1f0a6-1b22-449c-b4dd-f8feb7215554
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
07-21-2023
End Marketing Date: [10]
07-18-2027
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43742-2037?

The NDC code 43742-2037 is assigned by the FDA to the product Pollutox. It is commonly known by its generic name, 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, uranium nitricum, ozone. This pharmaceutical product is labeled by Deseret Biologicals, Inc. and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 43742-2037-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

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 Active Ingredients of this product?

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 - Inorganic and organic derivatives of sulfuric acid (H2SO4). The salts and esters of sulfuric acid are known as SULFATES and SULFURIC ACID ESTERS respectively.
  • 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 the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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 & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".