Household Detox Liquid
NDC 43742-2222

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43742-2222?
  4. Household Detox Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Household Detox (allium sativum, alumina, antipyrinum, benzinum, bisphenol a, carbolicum acidum, carboneum sulphuratum, diethylstilbestrol, dioxin, folliculinum, formalinum, glyphosate, methylparaben, naphthalinum, paraffinum, petroleum, phenacetinum, ptelea trifoliata, sodium carboxymethyl cellulose, teflon) 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 43742-2222 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43742-2222
Proprietary Name:
Household Detox
Non-Proprietary Name: [1]
Allium Sativum, Alumina, Antipyrinum, Benzinum, Bisphenol A, Carbolicum Acidum, Carboneum Sulphuratum, Diethylstilbestrol, Dioxin, Folliculinum, Formalinum, Glyphosate, Methylparaben, Naphthalinum, Paraffinum, Petroleum, Phenacetinum, Ptelea Trifoliata, Sodium Carboxymethyl Cellulose, Teflon
Substance Name: [2]
2,3,7,8-tetrachlorodibenzo-p-dioxin; Aluminum Oxide; Antipyrine; Benzene; Bisphenol A; Carbon Disulfide; Carboxymethylcellulose Sodium, Unspecified; Diethylstilbestrol; Estrone; Formaldehyde Solution; 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
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:
7f79058a-c35a-429a-be3c-4cff1d657087
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
12-13-2024
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43742-2222?

The NDC code 43742-2222 is assigned by the FDA to the product Household Detox. It is commonly known by its generic name, allium sativum, alumina, antipyrinum, benzinum, bisphenol a, carbolicum acidum, carboneum sulphuratum, diethylstilbestrol, dioxin, folliculinum, formalinum, glyphosate, methylparaben, naphthalinum, paraffinum, petroleum, phenacetinum, ptelea trifoliata, sodium carboxymethyl cellulose, teflon. 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: 43742-2222-1. 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.
  • 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 18 [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 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 SOLUTION 12 [hp_X]/mL
  • 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 - used as a preservative in cosmetics but potentiates UV-induced damage of skin; RN given refers to parent cpd
  • NAPHTHALENE 12 [hp_X]/mL - Two-ring crystalline hydrocarbons isolated from coal tar. They are used as intermediates in chemical synthesis, as insect repellents, fungicides, lubricants, preservatives, and, formerly, as topical antiseptics.
  • 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 14 [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 - Benzene derivatives that include one or more hydroxyl groups attached to the ring structure.
  • 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 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:

Which are the Pharmacologic Classes of this product?

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.

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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 Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
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".