NDC 43742-1227 Lymph Drainage

Citrus Limonum, Echinacea (angustifolia), Scrophularia Nodosa, Teucrium Scorodonia, Baptisia Tinctoria, Pinus Sylvestris, Zincum Gluconicum, Phytolacca Decandra, Thuja Occidentalis, Capsicum Annuum, Copper Gluconate, Manganese Gluconate, Aranea Diadema, Arsenicum Iodatum, Carpinus Betulus, Flos, Centaurium Umbellatum, Flos, Larix Decidua, Flos, Lymph Node (suis), Spleen (suis), Thymus (suis), Tabacum, Lachesis Mutus

NDC Product Code 43742-1227

NDC CODE: 43742-1227

Proprietary Name: Lymph 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: Citrus Limonum, Echinacea (angustifolia), Scrophularia Nodosa, Teucrium Scorodonia, Baptisia Tinctoria, Pinus Sylvestris, Zincum Gluconicum, Phytolacca Decandra, Thuja Occidentalis, Capsicum Annuum, Copper Gluconate, Manganese Gluconate, Aranea Diadema, Arsenicum Iodatum, Carpinus Betulus, Flos, Centaurium Umbellatum, Flos, Larix Decidua, Flos, Lymph Node (suis), Spleen (suis), Thymus (suis), Tabacum, Lachesis Mutus 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Drug uses not available

NDC Code Structure

  • 43742 - Deseret Biologicals

NDC 43742-1227-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Lymph Drainage with NDC 43742-1227 is a a human over the counter drug product labeled by Deseret Biologicals. The generic name of Lymph Drainage is citrus limonum, echinacea (angustifolia), scrophularia nodosa, teucrium scorodonia, baptisia tinctoria, pinus sylvestris, zincum gluconicum, phytolacca decandra, thuja occidentalis, capsicum annuum, copper gluconate, manganese gluconate, aranea diadema, arsenicum iodatum, carpinus betulus, flos, centaurium umbellatum, flos, larix decidua, flos, lymph node (suis), spleen (suis), thymus (suis), tabacum, lachesis mutus. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biologicals

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.

Lymph 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.

  • LEMON JUICE 1 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 1 [hp_X]/mL
  • SCROPHULARIA NODOSA 1 [hp_X]/mL
  • TEUCRIUM SCORODONIA FLOWERING TOP 1 [hp_X]/mL
  • BAPTISIA TINCTORIA ROOT 1 [hp_X]/mL
  • PINUS SYLVESTRIS LEAFY TWIG 3 [hp_X]/mL
  • ZINC GLUCONATE 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 4 [hp_X]/mL
  • CAPSICUM 6 [hp_X]/mL
  • COPPER GLUCONATE 6 [hp_X]/mL
  • MANGANESE GLUCONATE 6 [hp_X]/mL
  • ARANEUS DIADEMATUS 8 [hp_X]/mL
  • ARSENIC TRIIODIDE 8 [hp_X]/mL
  • CARPINUS BETULUS FLOWER 8 [hp_X]/mL
  • CENTAURIUM ERYTHRAEA FLOWER 8 [hp_X]/mL
  • LARIX DECIDUA FLOWERING TOP 8 [hp_X]/mL
  • SUS SCROFA LYMPH 8 [hp_X]/mL
  • SUS SCROFA SPLEEN 8 [hp_X]/mL
  • SUS SCROFA THYMUS 8 [hp_X]/mL
  • TOBACCO LEAF 9 [hp_X]/mL
  • LACHESIS MUTA VENOM 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.
  • 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
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: 05-25-2018 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: 07-25-2023 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.

Lymph Drainage Product Label Images

Lymph 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:

Citrus Limonum 1X, Echinacea (Angustifolia) 1X, Scrophularia Nodosa 1X, Teucrium Scorodonia 1X, Baptisia Tinctoria 1X, 3X, Pinus Sylvestris 3X, Zincum Gluconicum 3X, Phytolacca Decandra 4X, Thuja Occidentalis 4X, Capsicum Annuum 6X, Copper Gluconate 6X, Manganese Gluconate 6X, Aranea Diadema 8X, Arsenicum Iodatum 8X, Carpinus Betulus, Flos 8X, Centaurium Umbellatum, Flos 8X, Larix Decidua, Flos 8X, Lymph Node (Suis) 8X, Spleen (Suis) 8X, Thymus (Suis) 8X, Tabacum 9X, Lachesis Mutus 12X.

Homeopathic Indications:

For the temporary relief of symptoms related to drainage of the lymph, such as fatigue, and loss of energy.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of symptoms related to drainage of the lymph, such as fatigue, and loss of energy.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

Keep out of reach of children. In case of overdose, contact physician or a 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 physician or a 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 43742-1227-1HOMEOPATHICLYMPH DRAINAGE2 FL OZ (60 ml)

* Please review the disclaimer below.