Vascuflow Liquid
NDC 43742-1554

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1554?
  4. Vascuflow Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Vascuflow (melatonin, l-arginine, l-citrulline, ubidecarenonum, squalene, calcarea carbonica, cholesterinum, coumarinum, formalinum, gelsemium sempervirens, alpha-lipoicum acidum, mercurius corrosivus, plumbum metallicum, pantothenic acid, glonoinum, lycopodium clavatum, phosphorus, berberis vulgaris, red yeast rice, nitric oxide, proteus (morgani), rhus tox) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc.. This medication is typically used as a allergens [cs]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-1554 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43742-1554
Proprietary Name:
Vascuflow
Non-Proprietary Name: [1]
Melatonin, L-arginine, L-citrulline, Ubidecarenonum, Squalene, Calcarea Carbonica, Cholesterinum, Coumarinum, Formalinum, Gelsemium Sempervirens, Alpha-lipoicum Acidum, Mercurius Corrosivus, Plumbum Metallicum, Pantothenic Acid, Glonoinum, Lycopodium Clavatum, Phosphorus, Berberis Vulgaris, Red Yeast Rice, Nitric Oxide, Proteus (morgani), Rhus Tox
Substance Name: [2]
Arginine; Berberis Vulgaris Root Bark; Cholesterol; Citrulline; Coumarin; Formaldehyde; Gelsemium Sempervirens Root; Lead; Lycopodium Clavatum Spore; Melatonin; Mercuric Chloride; Monascus Purpureus; Nitric Oxide; Nitroglycerin; Oyster Shell Calcium Carbonate, Crude; Pantothenic Acid; Phosphorus; Proteus Morganii; Squalene; Thioctic Acid; Toxicodendron Pubescens Leaf; Ubidecarenone
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

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.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Deseret Biologicals, Inc.
Labeler Code:
43742
Product Label ID:
1ca5d57d-7cf0-4b9a-afa0-767dca99864d
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
09-06-2019
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43742-1554?

The NDC code 43742-1554 is assigned by the FDA to the product Vascuflow. It is commonly known by its generic name, melatonin, l-arginine, l-citrulline, ubidecarenonum, squalene, calcarea carbonica, cholesterinum, coumarinum, formalinum, gelsemium sempervirens, alpha-lipoicum acidum, mercurius corrosivus, plumbum metallicum, pantothenic acid, glonoinum, lycopodium clavatum, phosphorus, berberis vulgaris, red yeast rice, nitric oxide, proteus (morgani), rhus tox. This pharmaceutical product is labeled by Deseret Biologicals, Inc. and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 43742-1554-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

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. 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.

What are Active Ingredients of this product?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • ARGININE 6 [hp_X]/mL - An essential amino acid that is physiologically active in the L-form.
  • BERBERIS VULGARIS ROOT BARK 8 [hp_C]/mL
  • CHOLESTEROL 8 [hp_X]/mL - The principal sterol of all higher animals, distributed in body tissues, especially the brain and spinal cord, and in animal fats and oils.
  • CITRULLINE 6 [hp_X]/mL - The active metabolite of FOLIC ACID. Leucovorin is used principally as an antidote to FOLIC ACID ANTAGONISTS.
  • COUMARIN 8 [hp_X]/mL - Synthetic or naturally occurring substances related to coumarin, the delta-lactone of coumarinic acid.
  • FORMALDEHYDE 8 [hp_X]/mL - A highly reactive aldehyde gas formed by oxidation or incomplete combustion of hydrocarbons. In solution, it has a wide range of uses: in the manufacture of resins and textiles, as a disinfectant, and as a laboratory fixative or preservative. Formaldehyde solution (formalin) is considered a hazardous compound, and its vapor toxic. (From Reynolds, Martindale The Extra Pharmacopoeia, 30th ed, p717)
  • GELSEMIUM SEMPERVIRENS ROOT 8 [hp_X]/mL
  • LEAD 8 [hp_X]/mL - A soft, grayish metal with poisonous salts; atomic number 82, atomic weight 207.2, symbol Pb.
  • LYCOPODIUM CLAVATUM SPORE 6 [hp_C]/mL
  • MELATONIN 6 [hp_X]/mL - A biogenic amine that is found in animals and plants. In mammals, melatonin is produced by the PINEAL GLAND. Its secretion increases in darkness and decreases during exposure to light. Melatonin is implicated in the regulation of SLEEP, mood, and REPRODUCTION. Melatonin is also an effective antioxidant.
  • MERCURIC CHLORIDE 8 [hp_X]/mL - Mercury chloride (HgCl2). A highly toxic compound that volatizes slightly at ordinary temperature and appreciably at 100 degrees C. It is corrosive to mucous membranes and used as a topical antiseptic and disinfectant.
  • MONASCUS PURPUREUS 8 [hp_C]/mL - A genus in the family Monascaceae, order EUROTIALES. One species, Monascus purpureus, has multiple uses in traditional Chinese medicine (MEDICINE, CHINESE TRADITIONAL).
  • NITRIC OXIDE 12 [hp_C]/mL - A free radical gas produced endogenously by a variety of mammalian cells, synthesized from ARGININE by NITRIC OXIDE SYNTHASE. Nitric oxide is one of the ENDOTHELIUM-DEPENDENT RELAXING FACTORS released by the vascular endothelium and mediates VASODILATION. It also inhibits platelet aggregation, induces disaggregation of aggregated platelets, and inhibits platelet adhesion to the vascular endothelium. Nitric oxide activates cytosolic GUANYLATE CYCLASE and thus elevates intracellular levels of CYCLIC GMP.
  • NITROGLYCERIN 6 [hp_C]/mL - A volatile vasodilator which relieves ANGINA PECTORIS by stimulating GUANYLATE CYCLASE and lowering cytosolic calcium. It is also sometimes used for TOCOLYSIS and explosives.
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X]/mL
  • PANTOTHENIC ACID 10 [hp_X]/mL - A butyryl-beta-alanine that can also be viewed as pantoic acid complexed with BETA ALANINE. It is incorporated into COENZYME A and protects cells against peroxidative damage by increasing the level of GLUTATHIONE.
  • PHOSPHORUS 6 [hp_C]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
  • PROTEUS MORGANII 30 [hp_C]/mL
  • SQUALENE 8 [hp_X]/mL - A natural 30-carbon triterpene.
  • THIOCTIC ACID 8 [hp_X]/mL - An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS.
  • TOXICODENDRON PUBESCENS LEAF 30 [hp_C]/mL
  • UBIDECARENONE 6 [hp_X]/mL

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are the Inactive Ingredients associated UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes of this product?

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Product & Regulatory Definitions
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.
What is the Substance Name? An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".