NDC 43742-0647 Systemic Drainage

Alfalfa, Avena Sativa, Citrus Limonum, Glycyrrhiza Glabra, Uva-ursi, Taraxacum Officinale, Galium Aparine, Schisandra Chinensis, Solid Ago Virgaurea, Tabacum, Tylophora Asthmatica, Berberis Vulgaris, Chelidonium Majus, Hepar Suis, Intestine (suis), Kidney (suis), Lung (suis), Lymph Node (suis), Magnesium Gluconate, Nux Vomica, Potassium Gluconate, Zincum Gluconicum, Sarcolacticum Acidum, Lacticum Acidum

NDC Product Code 43742-0647

NDC Code: 43742-0647

Proprietary Name: Systemic Drainage 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: Alfalfa, Avena Sativa, Citrus Limonum, Glycyrrhiza Glabra, Uva-ursi, Taraxacum Officinale, Galium Aparine, Schisandra Chinensis, Solid Ago Virgaurea, Tabacum, Tylophora Asthmatica, Berberis Vulgaris, Chelidonium Majus, Hepar Suis, Intestine (suis), Kidney (suis), Lung (suis), Lymph Node (suis), Magnesium Gluconate, Nux Vomica, Potassium Gluconate, Zincum Gluconicum, Sarcolacticum Acidum, Lacticum Acidum 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.
    • 43742-0647 - Systemic Drainage

NDC 43742-0647-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Systemic Drainage with NDC 43742-0647 is a a human prescription drug product labeled by Deseret Biologicals, Inc.. The generic name of Systemic Drainage is alfalfa, avena sativa, citrus limonum, glycyrrhiza glabra, uva-ursi, taraxacum officinale, galium aparine, schisandra chinensis, solid ago virgaurea, tabacum, tylophora asthmatica, berberis vulgaris, chelidonium majus, hepar suis, intestine (suis), kidney (suis), lung (suis), lymph node (suis), magnesium gluconate, nux vomica, potassium gluconate, zincum gluconicum, sarcolacticum acidum, lacticum acidum. 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 Prescription 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.

Systemic Drainage 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.

  • ALFALFA 1 [hp_X]/mL
  • AVENA SATIVA FLOWERING TOP 1 [hp_X]/mL
  • LEMON JUICE 1 [hp_X]/mL
  • GLYCYRRHIZA GLABRA 1 [hp_X]/mL
  • ARCTOSTAPHYLOS UVA-URSI LEAF 1 [hp_X]/mL
  • TARAXACUM OFFICINALE 2 [hp_X]/mL
  • GALIUM APARINE 3 [hp_X]/mL
  • SCHISANDRA CHINENSIS FRUIT 3 [hp_X]/mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 3 [hp_X]/mL
  • TOBACCO LEAF 3 [hp_X]/mL
  • TYLOPHORA INDICA LEAF 3 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 6 [hp_X]/mL
  • CHELIDONIUM MAJUS 6 [hp_X]/mL
  • PORK LIVER 6 [hp_X]/mL
  • PORK INTESTINE 6 [hp_X]/mL
  • PORK KIDNEY 6 [hp_X]/mL
  • SUS SCROFA LUNG 6 [hp_X]/mL
  • SUS SCROFA LYMPH 6 [hp_X]/mL
  • MAGNESIUM GLUCONATE 6 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/mL
  • POTASSIUM GLUCONATE 6 [hp_X]/mL
  • ZINC GLUCONATE 6 [hp_X]/mL
  • LACTIC ACID, L- 8 [hp_X]/mL
  • LACTIC ACID, DL- 12 [hp_X]/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.

Pharmacological Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Allergens - [CS]
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]
  • Potassium Compounds - [CS]
  • Potassium Salt - [EPC] (Established Pharmacologic Class)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
  • Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Allergens - [CS]
  • Dietary Proteins - [CS]
  • Plant Proteins - [CS]
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Allergens - [CS]
  • Plant Proteins - [CS]

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: 11-03-2015 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: 02-22-2023 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.

Systemic Drainage Product Label Images

Systemic Drainage 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:

Alfalfa 1X, Avena Sativa 1X, Citrus Limonum 1X, Glycyrrhiza Glabra 1X, Uva-Ursi 1X, Taraxacum Officinale 2X, Galium Aparine 3X, Schisandra Chinensis 3X, Solidago Virgaurea 3X, Tabacum 3X, Tylophora Asthmatica 3X, Berberis Vulgaris 6X, Chelidonium Majus 6X, Hepar Suis 6X, Intestine (Suis) 6X, Kidney (Suis) 6X, Lung (Suis) 6X, Lymph Node (Suis) 6X, Magnesium Gluconate 6X, Nux Vomica 6X, Potassium Gluconate 6X, Zincum Gluconicum 6X, Sarcolacticum Acidum 8X, Lacticum Acidum 12X

Homeopathic Indications:

For temporary relief of symptoms relating to systemic drainage and cellular detox such as fatigue, low energy, headaches and body aches.****These statements are based upon homeopathic principles.  They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms relating to systemic drainage and cellular detox such as fatigue, low energy, headaches and body aches.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Keep Out Of Reach Of Children:

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

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.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Dist. By: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070 www.desbio.com

Package Label Display:

DESBIONDC 43742-0647-1HOMEOPATHICSYSTEMIC DRAINAGE2 FL OZ (30 ml)

* Please review the disclaimer below.

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