NDC 43742-0581 Advanced Detox Core Formula

Dulcamara, Echinacea Angustifolia, Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbic Acid, Coccus Cacti, Conium Maculatum, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Pulsatilla (vulgaris), Sarcolacticum Acidum, Lymph Node (suis), Sulphur, Glandula Suprarenalis Suis, L-phenylalanine, Calcarea Phosphorica, Ferrum Phosphoricum, Hepar Suis, Hypothalamus (suis), Spleen (suis), Cortisone Aceticum, Mercurius Solubilis, Baryta Carbonica, Tonsil (suis), Funiculus Umbilicalis Suis, Gaertner Bacillus,

NDC Product Code 43742-0581

NDC CODE: 43742-0581

Proprietary Name: Advanced 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: Dulcamara, Echinacea Angustifolia, Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbic Acid, Coccus Cacti, Conium Maculatum, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Pulsatilla (vulgaris), Sarcolacticum Acidum, Lymph Node (suis), Sulphur, Glandula Suprarenalis Suis, L-phenylalanine, Calcarea Phosphorica, Ferrum Phosphoricum, Hepar Suis, Hypothalamus (suis), Spleen (suis), Cortisone Aceticum, Mercurius Solubilis, Baryta Carbonica, Tonsil (suis), Funiculus Umbilicalis Suis, Gaertner Bacillus, 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.

NDC 43742-0581-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Advanced Detox Core Formula with NDC 43742-0581 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Advanced Detox Core Formula is dulcamara, echinacea angustifolia, aesculus hippocastanum, antimonium tartaricum, ascorbic acid, coccus cacti, conium maculatum, galium aparine, gentiana lutea, geranium robertianum, pulsatilla (vulgaris), sarcolacticum acidum, lymph node (suis), sulphur, glandula suprarenalis suis, l-phenylalanine, calcarea phosphorica, ferrum phosphoricum, hepar suis, hypothalamus (suis), spleen (suis), cortisone aceticum, mercurius solubilis, baryta carbonica, tonsil (suis), funiculus umbilicalis suis, gaertner bacillus, . 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.

Advanced 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.

  • SOLANUM DULCAMARA TOP 4 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 4 [hp_X]/mL
  • HORSE CHESTNUT 6 [hp_X]/mL
  • ANTIMONY POTASSIUM TARTRATE 6 [hp_X]/mL
  • ASCORBIC ACID 6 [hp_X]/mL
  • PROTORTONIA CACTI 6 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 6 [hp_X]/mL
  • GALIUM APARINE 6 [hp_X]/mL
  • GENTIANA LUTEA ROOT 6 [hp_X]/mL
  • GERANIUM ROBERTIANUM 6 [hp_X]/mL
  • PULSATILLA VULGARIS 6 [hp_X]/mL
  • LACTIC ACID, L- 6 [hp_X]/mL
  • SUS SCROFA LYMPH 8 [hp_X]/mL
  • SULFUR 8 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
  • PHENYLALANINE 10 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 10 [hp_X]/mL
  • FERROSOFERRIC PHOSPHATE 10 [hp_X]/mL
  • PORK LIVER 10 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS 10 [hp_X]/mL
  • SUS SCROFA SPLEEN 10 [hp_X]/mL
  • CORTISONE ACETATE 13 [hp_X]/mL
  • MERCURIUS SOLUBILIS 13 [hp_X]/mL
  • BARIUM CARBONATE 28 [hp_X]/mL
  • SUS SCROFA TONSIL 6 [hp_C]/mL
  • SUS SCROFA UMBILICAL CORD 6 [hp_C]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 9 [hp_C]/mL
  • LIOTHYRONINE 10 [hp_C]/mL
  • SUS SCROFA BONE MARROW 12 [hp_C]/mL
  • ESCHERICHIA COLI 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: 06-15-2015 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: 06-21-2022 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Advanced Detox Core Formula Product Label Images

Advanced 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:

Dulcamara 4X, Echinacea Angustifolia 4X, Aesculus Hippocastanum 6X, Antimonium Tartaricum 6X, Ascorbic Acid 6X, Coccus Cacti 6X, Conium Maculatum 6X, Galium Aparine 6X, Gentiana Lutea 6X, Geranium Robertianum 6X, Pulsatilla (Vulgaris) 6X, Sarcolacticum Acidum 6X, Lymph Node (Suis) 8X, Sulphur 8X, Glandula Suprarenalis Suis 8X, 30X, 200X, L-Phenylalanine 8X, 30X, 200X, Calcarea Phosphorica 10X, Ferrum Phosphoricum 10X, Hepar Suis 10X, Hypothalamus (Suis) 10X, Spleen (Suis) 10X, Cortisone Aceticum 13X, Mercurius Solubilis 13X, Baryta Carbonica 28X, Tonsil (Suis) 6C, 30C, Funiculus Umbilicalis Suis 6C, 30C, Gaertner Bacillus (Bach) 9C, Triiodothyronine 10C, Medulla Ossis Suis 12C, Mutabile Bacillus (Bach) 30C.

Homeopathic Indications:

Temporary relief of symptoms related to improper breakdown and excretion of allergenic substances including chronic pain, fatigue, cramping and upper respiratory allergy.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Temporary relief of symptoms related to improper breakdown and excretion of allergenic substances including chronic pain, fatigue, cramping and upper respiratory allergy.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

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 to 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 84070800-827-9529               www.desbio.com

Package Label Display:

NAMBUDRIPAD'S ALLERGY ELIMINATION TECHNIQUESNAETNDC 43742-0581-1HOMEOPATHICADVANCED DETOXCore FormulaNet Contents 1 FL OZ (30 ML)DESBIO

* Please review the disclaimer below.