NDC 43742-0309 Basic Detox Core Formula

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

NDC Product Code 43742-0309

NDC Code: 43742-0309

Proprietary Name: Basic Detox Core Formula What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

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

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.
    • 43742-0309 - Basic Detox Core Formula

NDC 43742-0309-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Basic Detox Core Formula with NDC 43742-0309 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Basic Detox Core Formula is carduus marianus, chelidonium majus, cinchona officinalis, lycopodium clavatum, taraxacum officinale, veratrum album, avena sativa, cynara scolymus, methylcobalamin, menadione, alpha-lipoicum acidum, hepar suis, colon (suis), duodenum (suis), gallbladder (suis), intestine (suis), lymph node (suis), pancreas suis, thymus (suis), alpha-ketoglutaricum, cholesterinum, formicum acidum, glyoxal trimer dihydrate, histaminum hydrochloricum, malic acid, natrum oxalaceticum, sulphur, calcarea carbonica,. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biologicals, Inc.

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.

Product Type: Human Otc Drug 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.

Basic Detox Core Formula Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • MILK THISTLE 3 [hp_X]/mL
  • CHELIDONIUM MAJUS 4 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 4 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 4 [hp_X]/mL
  • TARAXACUM OFFICINALE 4 [hp_X]/mL
  • VERATRUM ALBUM ROOT 4 [hp_X]/mL
  • AVENA SATIVA FLOWERING TOP 6 [hp_X]/mL
  • CYNARA SCOLYMUS LEAF 6 [hp_X]/mL
  • METHYLCOBALAMIN 6 [hp_X]/mL
  • MENADIONE 6 [hp_X]/mL
  • .ALPHA.-LIPOIC ACID 8 [hp_X]/mL
  • PORK LIVER 8 [hp_X]/mL
  • SUS SCROFA COLON 8 [hp_X]/mL
  • SUS SCROFA DUODENUM 8 [hp_X]/mL
  • SUS SCROFA GALLBLADDER 8 [hp_X]/mL
  • PORK INTESTINE 8 [hp_X]/mL
  • SUS SCROFA LYMPH 8 [hp_X]/mL
  • SUS SCROFA PANCREAS 8 [hp_X]/mL
  • SUS SCROFA THYMUS 8 [hp_X]/mL
  • .ALPHA.-KETOGLUTARIC ACID 10 [hp_X]/mL
  • CHOLESTEROL 10 [hp_X]/mL
  • FORMIC ACID 10 [hp_X]/mL
  • GLYOXAL TRIMER DIHYDRATE 10 [hp_X]/mL
  • HISTAMINE DIHYDROCHLORIDE 10 [hp_X]/mL
  • MALIC ACID 10 [hp_X]/mL
  • SODIUM DIETHYL OXALACETATE 10 [hp_X]/mL
  • SULFUR 13 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 28 [hp_X]/mL
  • OROTIC ACID 7 [hp_C]/mL
  • PROTEUS MORGANII 30 [hp_C]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 08-28-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 08-10-2022 What is the End Marketing Date?
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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Basic Detox Core Formula Product Label Images

Basic Detox Core Formula Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Carduus Marianus 3X, Chelidonium Majus 4X, Cinchona Officinalis 4X, Lycopodium Clavatum 4X, Taraxacum Officinale 4X, Veratrum Album 4X, Avena Sativa 6X, Cynara Scolymus 6X, Methylcobalamin 6X, Menadione 6X, 8X, 30X, 200X, alpha-Lipoicum Acidum 8X, Hepar Suis 8X, Colon (Suis) 8X, 30X, 200X, Duodenum (Suis) 8X, 30X, 200X, Gallbladder (Suis) 8X, 30X, 200X, Intestine (Suis) 8X, 30X, 200X, Lymph Node (Suis) 8X, 30X, 200X, Pancreas Suis 8X, 30X, 200X, Thymus (Suis) 8X, 30X, 200X, alpha-Ketoglutaricum 10X, Cholesterinum 10X, Formicum Acidum 10X, Glyoxal Trimer Dihydrate10X, Histaminum Hydrochloricum 10X, Malic Acid 10X, Natrum Oxalaceticum 10X, Sulphur 13X, Calcarea Carbonica 28X, Oroticum Acidum 7C, Morgan Bacillus (Pure) 30C, 200C, Morgan Gaertner 30C, 200C.

Indications:

Temporary relief of symptoms related to improper breakdown and excretion of allergenic substances, including gastrointestinal, skin rashes, bowel disturbance and muscle cramping.

Temporary relief of symptoms related to improper breakdown and excretion of allergenic substances, including gastrointestinal, skin rashes, bowel disturbance and muscle cramping.

Warnings:

If pregnant or breast-feeding, or have any allergic reaction to trace minerals, or any chronic or recurring symptoms or illness, consult a health professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store at room temperature.Keep out of direct sunlight.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

Adults 3-10 drops under the tongue 3 times daily or as directed by your health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

DISTRIBUTED BY:Deseret Biologicals, Inc. Sandy, UT 84070800-827-9629            www.desbio.com

Package Label Display:

NAMBUDRIPAD'S ALLERGY ELIMINATION TECHNIQUESNAETNDC 43742-0309-1HOMEOPATHICBASIC DETOXCore FormulaNet Contents 1 FL OZ (30 ML)DESBIO

* Please review the disclaimer below.

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