Vascuflow

Cholesterinum, Formalinum, Gelsemium Sempervirens, Melatonin, Coumarinum, L-arginine, L-citrulline, Mercurius Corrosivus, Ubidecarenonum, Lanosterol, Mevalonolactone, Squalene, Calcarea Carbonica, Alpha-lipoicum Acidum, Plumbum Metallicum, Pantothenic Acid, Glonoinum, Lycopodium Clavatum, Phosphorus, Berberis Vulgaris, Red Yeast Rice, Nitric Oxide, Proteus (morgani), Rhus Tox

Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-0819

Vascuflow also known as Cholesterinum, Formalinum, Gelsemium Sempervirens, Melatonin, Coumarinum, L-arginine, L-citrulline, Mercurius Corrosivus, Ubidecarenonum, Lanosterol, Mevalonolactone, Squalene, Calcarea Carbonica, Alpha-lipoicum Acidum, Plumbum Metallicum, Pantothenic Acid, Glonoinum, Lycopodium Clavatum, Phosphorus, Berberis Vulgaris, Red Yeast Rice, Nitric Oxide, Proteus (morgani), Rhus Tox is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Vascuflow is 43742-0819. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Vascuflow drug includes Arginine - 6 [hp_X]/mL Berberis Vulgaris Root Bark - 8 [hp_C]/mL Cholesterol - 3 [hp_X]/mL Citrulline - 6 [hp_X]/mL Coumarin - 6 [hp_X]/mL Formaldehyde - 3 [hp_X]/mL Gelsemium Sempervirens Root - 6 [hp_X]/mL Lanosterol - 8 [hp_X]/mL Lead - 8 [hp_X]/mL Lycopodium Clavatum Spore - 6 [hp_C]/mL and more. The currest status of Vascuflow drug is Active.

Drug Information:

Drug NDC:	43742-0819
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:	Vascuflow
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:	Cholesterinum, Formalinum, Gelsemium Sempervirens, Melatonin, Coumarinum, L-arginine, L-citrulline, Mercurius Corrosivus, Ubidecarenonum, Lanosterol, Mevalonolactone, Squalene, Calcarea Carbonica, Alpha-lipoicum Acidum, Plumbum Metallicum, Pantothenic Acid, Glonoinum, Lycopodium Clavatum, Phosphorus, Berberis Vulgaris, Red Yeast Rice, Nitric Oxide, Proteus (morgani), Rhus Tox
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:	ARGININE - 6 [hp_X]/mL BERBERIS VULGARIS ROOT BARK - 8 [hp_C]/mL CHOLESTEROL - 3 [hp_X]/mL CITRULLINE - 6 [hp_X]/mL COUMARIN - 6 [hp_X]/mL FORMALDEHYDE - 3 [hp_X]/mL GELSEMIUM SEMPERVIRENS ROOT - 6 [hp_X]/mL LANOSTEROL - 8 [hp_X]/mL LEAD - 8 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE - 6 [hp_C]/mL Load more... MELATONIN - 6 [hp_X]/mL MERCURIC CHLORIDE - 6 [hp_X]/mL MEVALONOLACTONE - 8 [hp_X]/mL NITRIC OXIDE - 12 [hp_C]/mL NITROGLYCERIN - 6 [hp_C]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE - 8 [hp_X]/mL PANTOTHENIC ACID - 10 [hp_X]/mL PHOSPHORUS - 6 [hp_C]/mL PROTEUS MORGANII - 30 [hp_C]/mL RED YEAST - 8 [hp_C]/mL SQUALENE - 8 [hp_X]/mL THIOCTIC ACID - 8 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF - 30 [hp_C]/mL UBIDECARENONE - 6 [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 Jul, 2016
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	16 Aug, 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:	09 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, 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:	N0000185508 N0000175629 N0000184306 M0000728 N0000009909 N0000175940 N0000175415 M0014874
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	94ZLA3W45F 1TH8Q20J0U 97C5T2UQ7J 29VT07BGDA A4VZ22K1WT 1HG84L3525 639KR60Q1Q 1J05Z83K3M 2P299V784P C88X29Y479 Load more... JL5DK93RCL 53GH7MZT1R 661X270Z3L 31C4KY9ESH G59M7S0WS3 2E32821G6I 19F5HK2737 27YLU75U4W 56X6LID5ZY 1EU532DCW4 7QWM220FJH 73Y7P0K73Y 6IO182RP7A EJ27X76M46
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:	Standardized Chemical Allergen [EPC] Vasodilator [EPC] Nitrate Vasodilator [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] Vasodilation [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] Nitrates [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] Increased Histamine Release [PE] Nitrate Vasodilator [EPC] Nitrates [CS] Standardized Chemical Allergen [EPC] Vasodilation [PE] Vasodilator [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
43742-0819-1	30 mL in 1 BOTTLE, DROPPER (43742-0819-1)	26 Jul, 2016	16 Aug, 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

Vascuflow

Cholesterinum & more..

Liquid
Deseret Biologicals, Inc.
NDC: 43742-0819

Purpose:

Homeopathic indications: for the temporary relief of the symptoms of fatigue.** **these statements are based upon traditional homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

Vascuflow cholesterinum, formalinum, gelsemium sempervirens, melatonin, coumarinum, l-arginine, l-citrulline, mercurius corrosivus, ubidecarenonum, lanosterol, mevalonolactone, squalene, calcarea carbonica, alpha-lipoicum acidum, plumbum metallicum, pantothenic acid, glonoinum, lycopodium clavatum, phosphorus, berberis vulgaris, red yeast rice, nitric oxide, proteus (morgani), rhus tox cholesterol cholesterol formaldehyde formaldehyde gelsemium sempervirens root gelsemium sempervirens root melatonin melatonin coumarin coumarin arginine arginine citrulline citrulline mercuric chloride mercuric cation ubidecarenone ubidecarenone lanosterol lanosterol mevalonolactone mevalonolactone squalene squalene oyster shell calcium carbonate, crude oyster shell calcium carbonate, crude thioctic acid .alpha.-lipoic acid lead lead pantothenic acid pantothenic acid nitroglycerin nitroglycerin lycopodium clavatum spore lycopodium clavatum spore phosphorus phosphorus berberis vulgaris root bark berberis vulgaris root bark red yeast red yeast nitric oxide nitric oxide proteus morganii proteus morganii toxicodendron pubescens leaf toxicodendron pubescens leaf 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: des bio ndc 43742-0819-1 homeopathic vascuflow 1 fl oz (30 ml) vascuflow

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.