Lymph Drainage

Citrus Limonum, Echinacea (angustifolia), Scrophularia Nodosa, Teucrium Scorodonia, Baptisia Tinctoria, Phytolacca Decandra Pinus Sylvestris, Zincum Gluconicum, 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

Deseret Biologicals
Human Otc Drug
NDC 43742-0823

Lymph Drainage also known as Citrus Limonum, Echinacea (angustifolia), Scrophularia Nodosa, Teucrium Scorodonia, Baptisia Tinctoria, Phytolacca Decandra Pinus Sylvestris, Zincum Gluconicum, 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 is a human otc drug labeled by 'Deseret Biologicals'. National Drug Code (NDC) number for Lymph Drainage is 43742-0823. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Lymph Drainage drug includes Araneus Diadematus - 8 [hp_X]/mL Arsenic Triiodide - 8 [hp_X]/mL Baptisia Tinctoria Root - 1 [hp_X]/mL Capsicum - 6 [hp_X]/mL Carpinus Betulus Flower - 8 [hp_X]/mL Centaurium Erythraea Flower - 8 [hp_X]/mL Copper Gluconate - 6 [hp_X]/mL Echinacea Angustifolia - 1 [hp_X]/mL Lachesis Muta Venom - 12 [hp_X]/mL Larix Decidua Flowering Top - 8 [hp_X]/mL and more. The currest status of Lymph Drainage drug is Active.

Drug Information:

Drug NDC:	43742-0823
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Lymph Drainage
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Citrus Limonum, Echinacea (angustifolia), Scrophularia Nodosa, Teucrium Scorodonia, Baptisia Tinctoria, Phytolacca Decandra Pinus Sylvestris, Zincum Gluconicum, 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
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Deseret Biologicals
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ARANEUS DIADEMATUS - 8 [hp_X]/mL ARSENIC TRIIODIDE - 8 [hp_X]/mL BAPTISIA TINCTORIA ROOT - 1 [hp_X]/mL CAPSICUM - 6 [hp_X]/mL CARPINUS BETULUS FLOWER - 8 [hp_X]/mL CENTAURIUM ERYTHRAEA FLOWER - 8 [hp_X]/mL COPPER GLUCONATE - 6 [hp_X]/mL ECHINACEA ANGUSTIFOLIA - 1 [hp_X]/mL LACHESIS MUTA VENOM - 12 [hp_X]/mL LARIX DECIDUA FLOWERING TOP - 8 [hp_X]/mL Load more... LEMON JUICE - 1 [hp_X]/mL MANGANESE GLUCONATE - 6 [hp_X]/mL PHYTOLACCA AMERICANA ROOT - 3 [hp_X]/mL PINUS SYLVESTRIS LEAFY TWIG - 3 [hp_X]/mL SCROPHULARIA NODOSA - 1 [hp_X]/mL SUS SCROFA LYMPH - 8 [hp_X]/mL SUS SCROFA SPLEEN - 8 [hp_X]/mL SUS SCROFA THYMUS - 8 [hp_X]/mL TEUCRIUM SCORODONIA FLOWERING TOP - 1 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG - 4 [hp_X]/mL TOBACCO LEAF - 9 [hp_X]/mL ZINC GLUCONATE - 3 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	16 Aug, 2016
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	23 Apr, 2023
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.
Listing Expiration Date:	10 May, 2026
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Deseret Biologicals
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
NUI:	N0000185375 N0000185371 N0000175629 N0000184306 M0000728 M0006342 M0016962 M0022575 N0000185001
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	6T6CO7R3Z5 3029988O2T 5EF0HWI5WU 00UK7646FG 07YL55QKZ9 B204P54Z1F RV823G6G67 VB06AV5US8 VSW71SS07I 9UMZ642257 Load more... AGN709ANTJ 9YY2F980SV 11E6VI8VEG Q1RGP4UB73 7H443NUB2T 33A7VYU29L 92AMN5J79Y 7B69B0BD62 LOK3I16O7G 1NT28V9397 6YR2608RSU U6WSN5SQ1Z
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Non-Standardized Plant Allergenic Extract [EPC] Non-Standardized Food Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE] Increased IgG Production [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Dietary Proteins [CS] Plant Proteins [CS] Vegetable Proteins [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Cell-mediated Immunity [PE] Copper Absorption Inhibitor [EPC] Decreased Copper Ion Absorption [PE] Dietary Proteins [CS] Increased Histamine Release [PE] Increased IgG Production [PE] Magnetic Resonance Contrast Activity [MoA] Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] Paramagnetic Contrast Agent [EPC] Plant Proteins [CS] Vegetable Proteins [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
43742-0823-1	60 mL in 1 BOTTLE, DROPPER (43742-0823-1)	16 Aug, 2016	23 Apr, 2023	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Lymph Drainage

Citrus Limonum & more..

Liquid
Deseret Biologicals
NDC: 43742-0823

Purpose:

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.

Product Elements:

Lymph drainage citrus limonum, echinacea (angustifolia), scrophularia nodosa, teucrium scorodonia, baptisia tinctoria, phytolacca decandra pinus sylvestris, zincum gluconicum, 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 lemon juice lemon juice echinacea angustifolia echinacea angustifolia scrophularia nodosa scrophularia nodosa teucrium scorodonia flowering top teucrium scorodonia flowering top baptisia tinctoria root baptisia tinctoria root phytolacca americana root phytolacca americana root pinus sylvestris leafy twig pinus sylvestris leafy twig zinc gluconate zinc cation thuja occidentalis leafy twig thuja occidentalis leafy twig capsicum capsicum copper gluconate cupric cation manganese gluconate manganese cation (2+) araneus diadematus araneus diadematus arsenic triiodide arsenic cation (3+) carpinus betulus flower carpinus betulus flower centaurium erythraea flower centaurium erythraea flower larix decidua flowering top larix decidua flowering top sus scrofa lymph sus scrofa lymph sus scrofa spleen sus scrofa spleen sus scrofa thymus sus scrofa thymus tobacco leaf tobacco leaf lachesis muta venom lachesis muta venom water alcohol

Indications and Usage:

Warnings:

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.

Dosage and Administration:

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.

Package Label Principal Display Panel:

Package label display: desbio ndc 43742-0823-1 homeopathic lymph drainage 2 fl oz (60 ml) image description

Further Questions:

Questions: dist. by: deseret biologicals, inc. 469 w. parkland drive sandy, ut 84070 www.desbio.com

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.