Chemdetox

Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Trifolium Pratense, Glandula Suprarenalis Suis, Hepar Suis, Lymph Node (suis), Phytolacca Decandra, Thyroidinum (suis), Iridium Metallicum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum, Selenium Metallicum, Salicylicum Acidum, Adrenocorticotrophin, Cortisone Aceticum, Eugenol, Stearyl Alcohol, Xylitol, Folliculinum, Benzoicum Acidum, Chlorinum, Potassium Sorbate, Sorbitol, Resorcinum

Dr. Donna Restivo Dc
Human Otc Drug
NDC 62185-0047

Chemdetox also known as Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Trifolium Pratense, Glandula Suprarenalis Suis, Hepar Suis, Lymph Node (suis), Phytolacca Decandra, Thyroidinum (suis), Iridium Metallicum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum, Selenium Metallicum, Salicylicum Acidum, Adrenocorticotrophin, Cortisone Aceticum, Eugenol, Stearyl Alcohol, Xylitol, Folliculinum, Benzoicum Acidum, Chlorinum, Potassium Sorbate, Sorbitol, Resorcinum is a human otc drug labeled by 'Dr. Donna Restivo Dc'. National Drug Code (NDC) number for Chemdetox is 62185-0047. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Chemdetox drug includes Arctium Lappa Root - 3 [hp_X]/mL Arsenic Trioxide - 12 [hp_X]/mL Asarum Canadense Root - 12 [hp_X]/mL Berberis Vulgaris Root Bark - 3 [hp_X]/mL Butylbenzene - 30 [hp_X]/mL Carbon Disulfide - 12 [hp_X]/mL Chlorine - 30 [hp_X]/mL Glycyrrhiza Glabra - 3 [hp_X]/mL Iridium - 12 [hp_X]/mL Kerosene - 30 [hp_X]/mL and more. The currest status of Chemdetox drug is Active.

Drug Information:

Drug NDC:	62185-0047
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:	Chemdetox
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:	Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Trifolium Pratense, Glandula Suprarenalis Suis, Hepar Suis, Lymph Node (suis), Phytolacca Decandra, Thyroidinum (suis), Iridium Metallicum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum, Selenium Metallicum, Salicylicum Acidum, Adrenocorticotrophin, Cortisone Aceticum, Eugenol, Stearyl Alcohol, Xylitol, Folliculinum, Benzoicum Acidum, Chlorinum, Potassium Sorbate, Sorbitol, Resorcinum
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Dr. Donna Restivo Dc
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:	ARCTIUM LAPPA ROOT - 3 [hp_X]/mL ARSENIC TRIOXIDE - 12 [hp_X]/mL ASARUM CANADENSE ROOT - 12 [hp_X]/mL BERBERIS VULGARIS ROOT BARK - 3 [hp_X]/mL BUTYLBENZENE - 30 [hp_X]/mL CARBON DISULFIDE - 12 [hp_X]/mL CHLORINE - 30 [hp_X]/mL GLYCYRRHIZA GLABRA - 3 [hp_X]/mL IRIDIUM - 12 [hp_X]/mL KEROSENE - 30 [hp_X]/mL Load more... LYCOPODIUM CLAVATUM SPORE - 12 [hp_X]/mL NITRIC ACID - 12 [hp_X]/mL PHENOL - 12 [hp_X]/mL PHOSPHORUS - 12 [hp_X]/mL PHYTOLACCA AMERICANA ROOT - 8 [hp_X]/mL PORK LIVER - 8 [hp_X]/mL SELENIUM - 12 [hp_X]/mL SORBITOL - 30 [hp_X]/mL STILLINGIA SYLVATICA ROOT - 3 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED - 12 [hp_X]/mL SULFURIC ACID - 12 [hp_X]/mL SUS SCROFA ADRENAL GLAND - 8 [hp_X]/mL SUS SCROFA THYROID - 8 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER - 3 [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:	18 Mar, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	10 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:	Dr. Donna Restivo DC
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:	N0000185371 N0000185375 N0000175629 N0000184306 M0000728 M0006342 M0016962 N0000185001 M0516536
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	597E9BI3Z3 S7V92P67HO E2O4O7TQYK 1TH8Q20J0U S8XZ2901RZ S54S8B99E8 4R7X1O2820 2788Z9758H 44448S9773 1C89KKC04E Load more... C88X29Y479 411VRN1TV4 339NCG44TV 27YLU75U4W 11E6VI8VEG 6EC706HI7F H6241UJ22B 506T60A25R QBR70R4FBK 269XH13919 O40UQP6WCF 398IYQ16YV 6RV024OAUQ 4JS0838828
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 Food Allergenic Extract [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] Dietary Proteins [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] Dietary Proteins [CS] Increased Histamine Release [PE] Increased IgG Production [PE] Non-Standardized Food Allergenic Extract [EPC] 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
62185-0047-1	30 mL in 1 BOTTLE, DROPPER (62185-0047-1)	18 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

Chemdetox

Berberis Vulgaris & more..

Liquid
Dr. Donna Restivo DC
NDC: 62185-0047

Purpose:

Homeopathic indications: for temporary relief of symptoms related to chemical toxicity such as sleep disturbances, head discomfort, irregular bowel habits, memory difficulties, pain and weakness, trembling, nausea.** **these statements are based upon homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

Chemdetox berberis vulgaris, glycyrrhiza glabra, lappa major, stillingia sylvatica, trifolium pratense, glandula suprarenalis suis, hepar suis, lymph node (suis), phytolacca decandra, thyroidinum (suis), iridium metallicum, lycopodium clavatum, nitricum acidum, nux vomica, phosphoricum acidum, selenium metallicum, salicylicum acidum, adrenocorticotrophin, cortisone aceticum, eugenol, stearyl alcohol, xylitol, folliculinum, benzoicum acidum, chlorinum, potassium sorbate, sorbitol, resorcinum berberis vulgaris root bark berberis vulgaris root bark glycyrrhiza glabra glycyrrhiza glabra arctium lappa root arctium lappa root stillingia sylvatica root stillingia sylvatica root trifolium pratense flower trifolium pratense flower sus scrofa adrenal gland sus scrofa adrenal gland pork liver pork liver phytolacca americana root phytolacca americana root sus scrofa thyroid sus scrofa thyroid arsenic trioxide arsenic cation (3+) asarum canadense root asarum canadense root phenol phenol carbon disulfide carbon disulfide iridium iridium lycopodium clavatum spore lycopodium clavatum spore nitric acid nitric acid strychnos nux-vomica seed strychnos nux-vomica seed phosphorus phosphorus selenium selenium sulfuric acid sulfuric acid chlorine chlorine butylbenzene butylbenzene kerosene kerosene sorbitol sorbitol water alcohol

Indications and Usage:

Warnings:

Warnings: keep out of reach of children. in case of overdose, get medical help or contact 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: 10 drops under the tongue, 3 to 6 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: dr. donna restivo dc wellness consultant ndc 62185-0047-1 homeopathic chem detox 1 fl oz (30 ml) chemdetox

Further Questions:

Questions: distributed by dr. donna restivo dc, wellness consultant 822 south lake blvd. mahopac, new york 10541 www.mahopacmassage.com â¢ (845) 628-6286

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.