Household Detox

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

Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-1453

Household Detox also known as 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 is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Household Detox is 43742-1453. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Household Detox drug includes 2,3,7,8-tetrachlorodibenzo-p-dioxin - 36 [hp_X]/mL Aluminum Oxide - 12 [hp_X]/mL Antipyrine - 16 [hp_X]/mL Benzene - 12 [hp_X]/mL Bisphenol A - 12 [hp_X]/mL Carbon Disulfide - 9 [hp_X]/mL Carboxymethylcellulose Sodium, Unspecified Form - 12 [hp_X]/mL Diethylstilbestrol - 15 [hp_C]/mL Estrone - 12 [hp_X]/mL Formaldehyde - 12 [hp_X]/mL and more. The currest status of Household Detox drug is Active.

Drug Information:

Drug NDC:	43742-1453
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Household Detox
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	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
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Deseret Biologicals, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN - 36 [hp_X]/mL ALUMINUM OXIDE - 12 [hp_X]/mL ANTIPYRINE - 16 [hp_X]/mL BENZENE - 12 [hp_X]/mL BISPHENOL A - 12 [hp_X]/mL CARBON DISULFIDE - 9 [hp_X]/mL CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM - 12 [hp_X]/mL DIETHYLSTILBESTROL - 15 [hp_C]/mL ESTRONE - 12 [hp_X]/mL FORMALDEHYDE - 12 [hp_X]/mL Load more... GARLIC - 6 [hp_X]/mL GLYPHOSATE - 12 [hp_X]/mL KEROSENE - 8 [hp_X]/mL METHYLPARABEN - 12 [hp_X]/mL NAPHTHALENE - 12 [hp_X]/mL PARAFFIN - 12 [hp_X]/mL PHENACETIN - 12 [hp_X]/mL PHENOL - 12 [hp_X]/mL POLYTETRAFLUOROETHYLENE - 33 [hp_C]/mL PTELEA TRIFOLIATA BARK - 6 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	19 Mar, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	15 May, 2026
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.
Listing Expiration Date:	31 Dec, 2024
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Deseret Biologicals, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
NUI:	N0000185508 N0000175629 N0000184306 M0000728 N0000185371 M0006342 M0016962
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	DO80M48B6O LMI26O6933 T3CHA1B51H J64922108F MLT3645I99 S54S8B99E8 K679OBS311 731DCA35BT 2DI9HA706A 1HG84L3525 Load more... V1V998DC17 4632WW1X5A 1C89KKC04E A2I8C7HI9T 2166IN72UN I9O0E3H2ZE ER0CTH01H9 339NCG44TV E1NC1JVS3O 5KQR6FTT0D
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Standardized Chemical Allergen [EPC] Non-Standardized Food Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Dietary Proteins [CS] Plant Proteins [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Cell-mediated Immunity [PE] Dietary Proteins [CS] Increased Histamine Release [PE] Non-Standardized Food Allergenic Extract [EPC] Plant Proteins [CS] Standardized Chemical Allergen [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
43742-1453-1	30 mL in 1 BOTTLE, DROPPER (43742-1453-1)	19 Mar, 2019	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Household Detox

Ptelea Trifoliata & more..

Liquid
Deseret Biologicals, Inc.
NDC: 43742-1453

Purpose:

Homeopathic indications: 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.

Product Elements:

Household detox 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 ptelea trifoliata bark ptelea trifoliata bark garlic garlic kerosene kerosene carbon disulfide carbon disulfide aluminum oxide aluminum oxide benzene benzene bisphenol a bisphenol a phenol phenol formaldehyde formaldehyde glyphosate glyphosate methylparaben methylparaben naphthalene naphthalene paraffin paraffin phenacetin phenacetin carboxymethylcellulose sodium, unspecified form carboxymethylcellulose estrone estrone antipyrine antipyrine 2,3,7,8-tetrachlorodibenzo-p-dioxin 2,3,7,8-tetrachlorodibenzo-p-dioxin diethylstilbestrol diethylstilbestrol polytetrafluoroethylene polytetrafluoroethylene water alcohol

Indications and Usage:

Warnings:

Warnings: keep out of reach of children. in case of overdose, contact physician or a poison control center right away. if pregnant or breast-feeding, ask a health professional before use. tamper seal: "sealed for your protection." do not use if seal is broken or missing.

Dosage and Administration:

Directions: 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.

Package Label Principal Display Panel:

Package label display: des bio ndc 43742-1453-1 homeopathic household detox 1 fl oz (30 ml) household detox

Further Questions:

Questions: dist. by: deseret biologicals, inc. 469 w. parkland drive sandy, ut 84070 www.desbio.com

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.