Detox I

Carduus Marianus, Chelidonium Majus, Lycopodium Clavatum, Taraxacum Officinale, Avena Sativa, Cynara Scolymus, Methylcobalamin, Menadione, Alpha-lipoicum Acidum, Cinchona Officinalis, Hepar Suis, Veratrum Album, Colon (suis), Duodenum (suis), Gallbladder (suis), Intestine (suis), Lymph Node (suis), Thymus (suis), Alpha-ketoglutaricum Acidum, Cholesterinum, Formicum Acidum, Glyoxal Trimer Dihydrate, Histaminum Hydrochloricum, Malic Acid, Natrum Oxalaceticum, Sulphur

Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-1477

Detox I also known as Carduus Marianus, Chelidonium Majus, Lycopodium Clavatum, Taraxacum Officinale, Avena Sativa, Cynara Scolymus, Methylcobalamin, Menadione, Alpha-lipoicum Acidum, Cinchona Officinalis, Hepar Suis, Veratrum Album, Colon (suis), Duodenum (suis), Gallbladder (suis), Intestine (suis), Lymph Node (suis), Thymus (suis), Alpha-ketoglutaricum Acidum, Cholesterinum, Formicum Acidum, Glyoxal Trimer Dihydrate, Histaminum Hydrochloricum, Malic Acid, Natrum Oxalaceticum, Sulphur is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Detox I is 43742-1477. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Detox I drug includes .alpha.-ketoglutaric Acid - 10 [hp_X]/mL .alpha.-lipoic Acid - 8 [hp_X]/mL Avena Sativa Flowering Top - 6 [hp_X]/mL Chelidonium Majus - 4 [hp_X]/mL Cholesterol - 10 [hp_X]/mL Cinchona Officinalis Bark - 8 [hp_X]/mL Cynara Scolymus Leaf - 6 [hp_X]/mL Formic Acid - 10 [hp_X]/mL Glyoxal Trimer Dihydrate - 10 [hp_X]/mL Histamine Dihydrochloride - 10 [hp_X]/mL and more. The currest status of Detox I drug is Active.

Drug Information:

Drug NDC:	43742-1477
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:	Detox I
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base:	Detox
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix:	I
A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
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:	Carduus Marianus, Chelidonium Majus, Lycopodium Clavatum, Taraxacum Officinale, Avena Sativa, Cynara Scolymus, Methylcobalamin, Menadione, Alpha-lipoicum Acidum, Cinchona Officinalis, Hepar Suis, Veratrum Album, Colon (suis), Duodenum (suis), Gallbladder (suis), Intestine (suis), Lymph Node (suis), Thymus (suis), Alpha-ketoglutaricum Acidum, Cholesterinum, Formicum Acidum, Glyoxal Trimer Dihydrate, Histaminum Hydrochloricum, Malic Acid, Natrum Oxalaceticum, Sulphur
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:	.ALPHA.-KETOGLUTARIC ACID - 10 [hp_X]/mL .ALPHA.-LIPOIC ACID - 8 [hp_X]/mL AVENA SATIVA FLOWERING TOP - 6 [hp_X]/mL CHELIDONIUM MAJUS - 4 [hp_X]/mL CHOLESTEROL - 10 [hp_X]/mL CINCHONA OFFICINALIS BARK - 8 [hp_X]/mL CYNARA SCOLYMUS LEAF - 6 [hp_X]/mL FORMIC ACID - 10 [hp_X]/mL GLYOXAL TRIMER DIHYDRATE - 10 [hp_X]/mL HISTAMINE DIHYDROCHLORIDE - 10 [hp_X]/mL Load more... LYCOPODIUM CLAVATUM SPORE - 4 [hp_X]/mL MALIC ACID - 10 [hp_X]/mL MENADIONE - 6 [hp_X]/mL METHYLCOBALAMIN - 6 [hp_X]/mL MILK THISTLE - 3 [hp_X]/mL OROTIC ACID MONOHYDRATE - 7 [hp_C]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE - 28 [hp_X]/mL PORK INTESTINE - 8 [hp_X]/mL PORK LIVER - 8 [hp_X]/mL PROTEUS MORGANII - 30 [hp_C]/mL SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS - 30 [hp_C]/mL SODIUM DIETHYL OXALACETATE - 10 [hp_X]/mL SULFUR - 13 [hp_X]/mL SUS SCROFA COLON - 8 [hp_X]/mL SUS SCROFA DUODENUM - 8 [hp_X]/mL SUS SCROFA GALLBLADDER - 8 [hp_X]/mL SUS SCROFA LYMPH - 8 [hp_X]/mL SUS SCROFA THYMUS - 8 [hp_X]/mL TARAXACUM OFFICINALE - 4 [hp_X]/mL VERATRUM ALBUM ROOT - 8 [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:	24 Apr, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	07 May, 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:	07 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.
UNII:	8ID597Z82X 73Y7P0K73Y MA9CQJ3F7F 7E889U5RNN 97C5T2UQ7J S003A158SB B71UA545DE 0YIW783RG1 R6GJS0F9NZ 3POA0Q644U Load more... C88X29Y479 817L1N4CKP 723JX6CXY5 BR1SN1JS2W U946SH95EE 91532S02AO 2E32821G6I 40GMI0R60L 6EC706HI7F 56X6LID5ZY Y3V16D4PV4 6CA025Y4FG 70FD1KFU70 94J255A0UC P6J2SFT80O B6A98VOI9I 33A7VYU29L 7B69B0BD62 39981FM375 QNS6W5US1Z
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.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
43742-1477-1	30 mL in 1 BOTTLE, DROPPER (43742-1477-1)	24 Apr, 2019	07 May, 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

Detox I

Carduus Marianus & more..

Liquid
Deseret Biologicals, Inc.
NDC: 43742-1477

Purpose:

Homeopathic indications: for the temporary relief of symptoms related to digestive issues, such as, bloating, gas, occasional diarrhea, occasional constipation, fatigue, and stomach upset.** **these statements are based upon homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

Detox i carduus marianus, chelidonium majus, lycopodium clavatum, taraxacum officinale, avena sativa, cynara scolymus, methylcobalamin, menadione, alpha-lipoicum acidum, cinchona officinalis, hepar suis, veratrum album, colon (suis), duodenum (suis), gallbladder (suis), intestine (suis), lymph node (suis), thymus (suis), alpha-ketoglutaricum acidum, cholesterinum, formicum acidum, glyoxal trimer dihydrate, histaminum hydrochloricum, malic acid, natrum oxalaceticum, sulphur milk thistle milk thistle chelidonium majus chelidonium majus lycopodium clavatum spore lycopodium clavatum spore taraxacum officinale taraxacum officinale avena sativa flowering top avena sativa flowering top cynara scolymus leaf cynara scolymus leaf methylcobalamin methylcobalamin menadione menadione .alpha.-lipoic acid .alpha.-lipoic acid cinchona officinalis bark cinchona officinalis bark pork liver pork liver veratrum album root veratrum album root sus scrofa colon sus scrofa colon sus scrofa duodenum sus scrofa duodenum sus scrofa gallbladder sus scrofa gallbladder pork intestine pork intestine sus scrofa lymph sus scrofa lymph sus scrofa thymus sus scrofa thymus .alpha.-ketoglutaric acid .alpha.-ketoglutaric acid cholesterol cholesterol formic acid formic acid glyoxal trimer dihydrate glyoxal histamine dihydrochloride histamine malic acid malic acid sodium diethyl oxalacetate diethyl oxalacetate sulfur sulfur oyster shell calcium carbonate, crude oyster shell calcium carbonate, crude orotic acid monohydrate orotic acid salmonella enterica subsp. enterica serovar enteritidis salmonella enterica enterica serovar enteritidis proteus morganii proteus morganii 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 43742-1477-1 homeopathic detox i 1 fl oz (30 ml) detox i

Further Questions:

Questions: dist. by: deseret biologicals, inc. 469 w. parkland dr. 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.