NDC 43742-0572 Systemic Drainage

Alfalfa, Avena Sativa, Citrus Limonum, Glycyrrhiza Glabra, Uva-ursi, Taraxacum Officinale, Galium Aparine, Lobelia Inflata, Schisandra Chinensis, Solidago Virgaurea, 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 43742-0572

NDC Code: 43742-0572

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, Lobelia Inflata, Schisandra Chinensis, Solidago Virgaurea, 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.


Code Structure
  • 43742 - Deseret Biologicals, Inc.
    • 43742-0572 - Systemic Drainage

NDC 43742-0572-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Systemic Drainage with NDC 43742-0572 is a a human over the counter 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, lobelia inflata, schisandra chinensis, solidago virgaurea, 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 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.


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
  • LOBELIA INFLATA 3 [hp_X]/mL
  • SCHISANDRA CHINENSIS FRUIT 3 [hp_X]/mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 3 [hp_X]/mL
  • TYLOPHORA INDICA WHOLE 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.

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: 03-26-2015 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: 06-17-2020 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, Lobelia Inflata 3X, Schisandra Chinensis 3X, Solidago Virgaurea 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.

Indications:

For the temporary relief of symptoms relating to systemic drainage and cellular detox such as fatigue, low energy, headaches and body aches.

For the temporary relief of symptoms relating to systemic drainage and cellular detox such as fatigue, low energy, headaches and body aches.

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.

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 43742-0572-1HOMEOPATHICSYSTEMICDRAINAGE2 FL OZ (60 ml)

* Please review the disclaimer below.

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