Petrochemical Detox

Chelidonium Majus, Symphytum Officinale, Taraxacum Officinale, Trifolium Pratense, Acetone, Sodium Tripolyphosphate, Propylene Glycol, Sodium Benzene Sulfonate, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Arsenicum Album, Cadmium Sulphuratum, Gelsemium Sempervirens, Iridium Metallicum, Lycopodium Clavatum, Mercurius Solubilis, Nitricum Acidum, Nitricum Acidum, Nux Vomica, Petroleum, Phosphoricum Acidum, Platinum Metallicum, Latrodectus Mactans

Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-0915

Petrochemical Detox also known as Chelidonium Majus, Symphytum Officinale, Taraxacum Officinale, Trifolium Pratense, Acetone, Sodium Tripolyphosphate, Propylene Glycol, Sodium Benzene Sulfonate, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Arsenicum Album, Cadmium Sulphuratum, Gelsemium Sempervirens, Iridium Metallicum, Lycopodium Clavatum, Mercurius Solubilis, Nitricum Acidum, Nitricum Acidum, Nux Vomica, Petroleum, Phosphoricum Acidum, Platinum Metallicum, Latrodectus Mactans is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Petrochemical Detox is 43742-0915. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Petrochemical Detox drug includes Acetone - 9 [hp_X]/mL Ammonium Chloride - 9 [hp_X]/mL Arsenic Trioxide - 12 [hp_X]/mL Cadmium Sulfide - 12 [hp_X]/mL Chelidonium Majus - 3 [hp_X]/mL Comfrey Root - 6 [hp_X]/mL Gelsemium Sempervirens Root - 12 [hp_X]/mL Iridium - 12 [hp_X]/mL Kerosene - 12 [hp_X]/mL Latrodectus Mactans - 15 [hp_X]/mL and more. The currest status of Petrochemical Detox drug is Active.

Drug Information:

Drug NDC:	43742-0915
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:	Petrochemical 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:	Chelidonium Majus, Symphytum Officinale, Taraxacum Officinale, Trifolium Pratense, Acetone, Sodium Tripolyphosphate, Propylene Glycol, Sodium Benzene Sulfonate, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Arsenicum Album, Cadmium Sulphuratum, Gelsemium Sempervirens, Iridium Metallicum, Lycopodium Clavatum, Mercurius Solubilis, Nitricum Acidum, Nitricum Acidum, Nux Vomica, Petroleum, Phosphoricum Acidum, Platinum Metallicum, Latrodectus Mactans
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:	ACETONE - 9 [hp_X]/mL AMMONIUM CHLORIDE - 9 [hp_X]/mL ARSENIC TRIOXIDE - 12 [hp_X]/mL CADMIUM SULFIDE - 12 [hp_X]/mL CHELIDONIUM MAJUS - 3 [hp_X]/mL COMFREY ROOT - 6 [hp_X]/mL GELSEMIUM SEMPERVIRENS ROOT - 12 [hp_X]/mL IRIDIUM - 12 [hp_X]/mL KEROSENE - 12 [hp_X]/mL LATRODECTUS MACTANS - 15 [hp_X]/mL Load more... LYCOPODIUM CLAVATUM SPORE - 12 [hp_X]/mL MERCURIUS SOLUBILIS - 12 [hp_X]/mL NITRIC ACID - 12 [hp_X]/mL PHOSPHORIC ACID - 12 [hp_X]/mL PLATINUM - 12 [hp_X]/mL PROPYLENE GLYCOL - 9 [hp_X]/mL SODIUM BENZENESULFONATE - 9 [hp_X]/mL SODIUM LAURYL SULFATE - 9 [hp_X]/mL SODIUM TRIPOLYPHOSPHATE - 9 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED - 12 [hp_X]/mL TARAXACUM OFFICINALE - 3 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER - 6 [hp_X]/mL TURPENTINE OIL - 9 [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:	28 Nov, 2016
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	10 Apr, 2024
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:	10 May, 2026
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:	N0000185375 N0000175629 N0000184306 N0000185001 M0000728 M0016962 M0516536
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	1364PS73AF 01Q9PC255D S7V92P67HO 057EZR4Z7Q 7E889U5RNN M9VVZ08EKQ 639KR60Q1Q 44448S9773 1C89KKC04E XJJ7QA858R Load more... C88X29Y479 324Y4038G2 411VRN1TV4 E4GA8884NN 49DFR088MY 6DC9Q167V3 K5RM14AZHX 368GB5141J 5HK03SA80J 269XH13919 39981FM375 4JS0838828 C5H0QJ6V7F
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:	Non-Standardized Plant 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] Increased IgG Production [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] Plant Proteins [CS] Seed Storage 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] Increased Histamine Release [PE] Increased IgG Production [PE] Non-Standardized Plant Allergenic Extract [EPC] Plant Proteins [CS] Seed Storage Proteins [CS]
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
43742-0915-1	30 mL in 1 BOTTLE, DROPPER (43742-0915-1)	28 Nov, 2016	10 Apr, 2024	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

Petrochemical Detox

Chelidonium Majus & more..

Liquid
Deseret Biologicals, Inc.
NDC: 43742-0915

Purpose:

Homeopathic indications: for the temporary relief of symptoms related to petrochemical toxicity including rash, fever, fatigue, headache, muscle and joint pain, and frequent colds.** **these statements are based upon traditional homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

Petrochemical detox chelidonium majus, symphytum officinale, taraxacum officinale, trifolium pratense, acetone, sodium tripolyphosphate, propylene glycol, sodium benzene sulfonate, ammonium muriaticum, sodium lauryl sulfate, terebinthina, arsenicum album, cadmium sulphuratum, gelsemium sempervirens, iridium metallicum, lycopodium clavatum, mercurius solubilis, nitricum acidum, nitricum acidum, nux vomica, petroleum, phosphoricum acidum, platinum metallicum, latrodectus mactans chelidonium majus chelidonium majus taraxacum officinale taraxacum officinale trifolium pratense flower trifolium pratense flower comfrey root comfrey root acetone acetone ammonium chloride ammonium cation propylene glycol propylene glycol sodium benzenesulfonate benzenesulfonic acid sodium lauryl sulfate lauryl sulfate sodium tripolyphosphate tripolyphosphate ion turpentine oil turpentine oil arsenic trioxide arsenic cation (3+) cadmium sulfide cadmium cation gelsemium sempervirens root gelsemium sempervirens root iridium iridium lycopodium clavatum spore lycopodium clavatum spore mercurius solubilis mercurius solubilis nitric acid nitric acid strychnos nux-vomica seed strychnos nux-vomica seed kerosene kerosene phosphoric acid phosphoric acid platinum platinum latrodectus mactans latrodectus mactans water alcohol

Indications and Usage:

Warnings:

Warnings: keep out of reach of children. in case of overdose, contact physician or 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 43742-0915-1 homeopathic petrochemical detox 1 fl oz (30 ml) petrochemical detox

Further Questions:

Questions: dist. by: deseret biologicals, inc. 469 w. parkland drive sandy, ut 84070 www.desbio.com *for a complete list of environmental isodes contact deseret biologicals, inc.

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.