NDC 43742-1453 Household Detox

Ptelea Trifoliata,Allium Sativum,Petroleum,Carboneum - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
43742-1453
Proprietary Name:
Household Detox
Non-Proprietary Name: [1]
Ptelea Trifoliata, Allium Sativum, Petroleum, Carboneum Sulphuratum, Alumina, Benzinum, Bisphenol A, Carbolicum Acidum, Formalinum, Glyphosate, Methylparaben, Naphthalinum, Paraffinum, Phenacetinum, Sodium Carboxymethyl Cellulose, Folliculinum, Antipyrinum, Dioxin, Diethylstilbestrol, Teflon
Substance Name: [2]
2,3,7,8-tetrachlorodibenzo-p-dioxin; Aluminum Oxide; Antipyrine; Benzene; Bisphenol A; Carbon Disulfide; Carboxymethylcellulose Sodium, Unspecified Form; Diethylstilbestrol; Estrone; Formaldehyde; Garlic; Glyphosate; Kerosene; Methylparaben; Naphthalene; Paraffin; Phenacetin; Phenol; Polytetrafluoroethylene; Ptelea Trifoliata Bark
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
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    03-19-2019
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 43742-1453-1

    Package Description: 30 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 43742-1453?

    The NDC code 43742-1453 is assigned by the FDA to the product Household Detox which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Household Detox is ptelea trifoliata, allium sativum, petroleum, carboneum sulphuratum, alumina, benzinum, bisphenol a, carbolicum acidum, formalinum, glyphosate, methylparaben, naphthalinum, paraffinum, phenacetinum, sodium carboxymethyl cellulose, folliculinum, antipyrinum, dioxin, diethylstilbestrol, teflon. 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 43742-1453-1 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 Household Detox?

    For the temporary relief of symptoms related to toxicity, such as headache, fatigue, body aches, and skin complaints.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the temporary relief of symptoms related to toxicity, such as headache, fatigue, body aches, and skin complaints.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

    What are Household Detox 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.
    • 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN 36 [hp_X]/mL
    • ALUMINUM OXIDE 12 [hp_X]/mL - An oxide of aluminum, occurring in nature as various minerals such as bauxite, corundum, etc. It is used as an adsorbent, desiccating agent, and catalyst, and in the manufacture of dental cements and refractories.
    • ANTIPYRINE 16 [hp_X]/mL - An analgesic and antipyretic that has been given by mouth and as ear drops. Antipyrine is often used in testing the effects of other drugs or diseases on drug-metabolizing enzymes in the liver. (From Martindale, The Extra Pharmacopoeia, 30th ed, p29)
    • 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.
    • BISPHENOL A 12 [hp_X]/mL
    • CARBON DISULFIDE 9 [hp_X]/mL - A colorless, flammable, poisonous liquid, CS2. It is used as a solvent, and is a counterirritant and has local anesthetic properties but is not used as such. It is highly toxic with pronounced CNS, hematologic, and dermatologic effects.
    • CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM 12 [hp_X]/mL
    • DIETHYLSTILBESTROL 15 [hp_C]/mL - A synthetic nonsteroidal estrogen used in the treatment of menopausal and postmenopausal disorders. It was also used formerly as a growth promoter in animals. According to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985), diethylstilbestrol has been listed as a known carcinogen. (Merck, 11th ed)
    • ESTRONE 12 [hp_X]/mL - An aromatized C18 steroid with a 3-hydroxyl group and a 17-ketone, a major mammalian estrogen. It is converted from ANDROSTENEDIONE directly, or from TESTOSTERONE via ESTRADIOL. In humans, it is produced primarily by the cyclic ovaries, PLACENTA, and the ADIPOSE TISSUE of men and postmenopausal women.
    • FORMALDEHYDE 12 [hp_X]/mL - A highly reactive aldehyde gas formed by oxidation or incomplete combustion of hydrocarbons. In solution, it has a wide range of uses: in the manufacture of resins and textiles, as a disinfectant, and as a laboratory fixative or preservative. Formaldehyde solution (formalin) is considered a hazardous compound, and its vapor toxic. (From Reynolds, Martindale The Extra Pharmacopoeia, 30th ed, p717)
    • GARLIC 6 [hp_X]/mL - A species of Allium used as a spice (SPICES) and traditional remedy. It contains alliin lyase and alliin, which is converted by alliin lyase to allicin, the pungent ingredient responsible for the aroma of fresh cut garlic.
    • GLYPHOSATE 12 [hp_X]/mL - Active compound in herbicidal formulations that inhibits 3-PHOSPHOSHIKIMATE 1-CARBOXYVINYLTRANSFERASE.
    • KEROSENE 8 [hp_X]/mL - A refined petroleum fraction used as a fuel as well as a solvent.
    • METHYLPARABEN 12 [hp_X]/mL
    • NAPHTHALENE 12 [hp_X]/mL
    • PARAFFIN 12 [hp_X]/mL - A mixture of solid hydrocarbons obtained from petroleum. It has a wide range of uses including as a stiffening agent in ointments, as a lubricant, and as a topical anti-inflammatory. It is also commonly used as an embedding material in histology.
    • PHENACETIN 12 [hp_X]/mL - A phenylacetamide that was formerly used in ANALGESICS but nephropathy and METHEMOGLOBINEMIA led to its withdrawal from the market. (From Smith and Reynard, Textbook of Pharmacology,1991, p431)
    • PHENOL 12 [hp_X]/mL - An antiseptic and disinfectant aromatic alcohol.
    • POLYTETRAFLUOROETHYLENE 33 [hp_C]/mL - Homopolymer of tetrafluoroethylene. Nonflammable, tough, inert plastic tubing or sheeting; used to line vessels, insulate, protect or lubricate apparatus; also as filter, coating for surgical implants or as prosthetic material. Synonyms: Fluoroflex; Fluoroplast; Ftoroplast; Halon; Polyfene; PTFE; Tetron.
    • PTELEA TRIFOLIATA BARK 6 [hp_X]/mL

    Which are Household Detox UNII Codes?

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

    Which are Household Detox 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 Household Detox?

    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".