Lung Drainage

Kali Muriaticum, Carbo Vegetabilis, Lung (suis), Mycoplasma Pneumoniae, Bryonia (alba), Gelsemium Sempervirens, Haemophilus Influenzae B, Pneumococcinum, Oxygenium, Antimonium Arsenicicum, Camphora, Chelidonium Majus, Chininum Muriaticum, Cuprum Metallicum, Ipecacuanha, Lobelia Purpurescens, Phosphorus, Senega Officinalis, Stannum Metallicum, Veratrum Viride

Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-1649

Lung Drainage also known as Kali Muriaticum, Carbo Vegetabilis, Lung (suis), Mycoplasma Pneumoniae, Bryonia (alba), Gelsemium Sempervirens, Haemophilus Influenzae B, Pneumococcinum, Oxygenium, Antimonium Arsenicicum, Camphora, Chelidonium Majus, Chininum Muriaticum, Cuprum Metallicum, Ipecacuanha, Lobelia Purpurescens, Phosphorus, Senega Officinalis, Stannum Metallicum, Veratrum Viride is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Lung Drainage is 43742-1649. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Lung Drainage drug includes Activated Charcoal - 8 [hp_X]/mL Antimony Arsenate - 30 [hp_X]/mL Bryonia Alba Root - 12 [hp_X]/mL Camphor (natural) - 30 [hp_X]/mL Chelidonium Majus Whole - 30 [hp_X]/mL Copper - 30 [hp_X]/mL Gelsemium Sempervirens Root - 12 [hp_X]/mL Haemophilus Influenzae Type B - 16 [hp_X]/mL Ipecac - 30 [hp_X]/mL Mycoplasma Pneumoniae - 12 [hp_X]/mL and more. The currest status of Lung Drainage drug is Active.

Drug Information:

Drug NDC:	43742-1649
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:	Lung 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:	Kali Muriaticum, Carbo Vegetabilis, Lung (suis), Mycoplasma Pneumoniae, Bryonia (alba), Gelsemium Sempervirens, Haemophilus Influenzae B, Pneumococcinum, Oxygenium, Antimonium Arsenicicum, Camphora, Chelidonium Majus, Chininum Muriaticum, Cuprum Metallicum, Ipecacuanha, Lobelia Purpurescens, Phosphorus, Senega Officinalis, Stannum Metallicum, Veratrum Viride
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Deseret Biologicals, Inc.
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:	ACTIVATED CHARCOAL - 8 [hp_X]/mL ANTIMONY ARSENATE - 30 [hp_X]/mL BRYONIA ALBA ROOT - 12 [hp_X]/mL CAMPHOR (NATURAL) - 30 [hp_X]/mL CHELIDONIUM MAJUS WHOLE - 30 [hp_X]/mL COPPER - 30 [hp_X]/mL GELSEMIUM SEMPERVIRENS ROOT - 12 [hp_X]/mL HAEMOPHILUS INFLUENZAE TYPE B - 16 [hp_X]/mL IPECAC - 30 [hp_X]/mL MYCOPLASMA PNEUMONIAE - 12 [hp_X]/mL Load more... OXYGEN - 16 [hp_X]/mL PHOSPHORUS - 30 [hp_X]/mL POLYGALA SENEGA ROOT - 30 [hp_X]/mL POTASSIUM CHLORIDE - 6 [hp_X]/mL PRATIA PURPURASCENS - 30 [hp_X]/mL QUININE HYDROCHLORIDE - 30 [hp_X]/mL STREPTOCOCCUS PNEUMONIAE - 16 [hp_X]/mL SUS SCROFA LUNG - 8 [hp_X]/mL TIN - 30 [hp_X]/mL VERATRUM VIRIDE ROOT - 30 [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:	26 Jun, 2020
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	10 May, 2026
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:	31 Dec, 2023
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, Inc.
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:	M0005152 N0000175831 N0000008595 N0000008924 N0000175830
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	2P3VWU3H10 WE3458XNFT T7J046YI2B N20HL7Q941 7E889U5RNN 789U1901C5 639KR60Q1Q F2TW0N64FI 62I3C8233L JQE470FAD0 Load more... S88TT14065 27YLU75U4W M7T6H7D4IF 660YQ98I10 901NKD188B 711S8Y0T33 BT6U234YR2 7GL3G1COB3 387GMG9FH5 197B3Q7T5Q
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:	Copper-containing Intrauterine Device [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:	Decreased Embryonic Implantation [PE] Decreased Sperm Motility [PE] Inhibit Ovum Fertilization [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:	Copper [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:	Antimalarial [EPC] Copper [CS] Copper-containing Intrauterine Device [EPC] Decreased Embryonic Implantation [PE] Decreased Sperm Motility [PE] Increased Large Intestinal Motility [PE] Inhibit Ovum Fertilization [PE] Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] Osmotic Activity [MoA] Osmotic Laxative [EPC] Potassium Compounds [CS] Potassium Salt [EPC]
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
43742-1649-1	30 mL in 1 BOTTLE, DROPPER (43742-1649-1)	26 Jun, 2020	N/A	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

Lung Drainage

Kali Muriaticum & more..

Liquid
Deseret Biologicals, Inc.
NDC: 43742-1649

Purpose:

Homeopathic indications: for temporary relief of symptoms related to drainage of lungs such as fatigue and cough.** **these statements are based upon homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

Lung drainage kali muriaticum, carbo vegetabilis, lung (suis), mycoplasma pneumoniae, bryonia (alba), gelsemium sempervirens, haemophilus influenzae b, pneumococcinum, oxygenium, antimonium arsenicicum, camphora, chelidonium majus, chininum muriaticum, cuprum metallicum, ipecacuanha, lobelia purpurescens, phosphorus, senega officinalis, stannum metallicum, veratrum viride potassium chloride potassium cation activated charcoal activated charcoal sus scrofa lung sus scrofa lung mycoplasma pneumoniae mycoplasma pneumoniae bryonia alba root bryonia alba root gelsemium sempervirens root gelsemium sempervirens root haemophilus influenzae type b haemophilus influenzae type b streptococcus pneumoniae streptococcus pneumoniae oxygen oxygen antimony arsenate arsenate ion camphor (natural) camphor (natural) chelidonium majus whole chelidonium majus quinine hydrochloride quinine copper copper ipecac ipecac pratia purpurascens pratia purpurascens phosphorus phosphorus polygala senega root polygala senega root tin tin veratrum viride root veratrum viride root water alcohol

Indications and Usage:

Warnings:

Warnings: keep out of reach of children . in case of overdose, contact a 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.

Dosage and Administration:

Directions: 3-10 drops under the tongue, 3 times a day or as directed by a health professional. consult a physician for use in children uner 12 years of age.

Package Label Principal Display Panel:

Package label display: des bio ndc 43742-1649-1 homeopathic lung drainage 1 fl oz (30 ml) lung drainage

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.