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NDC 64578-0095 Adaptopath

Adenosinum Cyclophosphoricum,Alpha-lipoicum Acidum,Argentum Metallicum,Avena - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64578-0095?
  4. Active Ingredients
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 64578-0095 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
64578-0095
Proprietary Name:
Adaptopath
Non-Proprietary Name: [1]
Adenosinum Cyclophosphoricum, Alpha-lipoicum Acidum, Argentum Metallicum, Avena Sativa, Capsicum Annuum, Citricum Acidum, Coenzyme A, Cuprum Metallicum, Ginkgo Biloba, Glandula Suprarenalis Suis, Glycyrrhiza Glabra, Hypothalamus (bovine), Iodium, Ledum Palustre, Manganum Aceticum, Nadidum, Natrum Carbonicum, Oleum Morrhuae, Phosphoricum Acidum, Picricum Acidum, Riboflavinum, Selenium Metallicum Sepia, Silicea, Thiaminum Hydrochloricum, Thyroidinum (bovine), Vanadium Metallicum
Substance Name: [2]
.alpha.-lipoic Acid; Adenosine Cyclic Phosphate; Anhydrous Citric Acid; Avena Sativa Flowering Top; Bos Taurus Hypothalamus; Capsicum; Cod Liver Oil; Coenzyme A; Copper; Ginkgo; Glycyrrhiza Glabra; Iodine; Ledum Palustre Twig; Manganese Acetate Tetrahydrate; Nadide; Phosphoric Acid; Picric Acid; Riboflavin; Selenium; Sepia Officinalis Juice; Silicon Dioxide; Silver; Sodium Carbonate; Sus Scrofa Adrenal Gland; Thiamine Hydrochloride; Thyroid, Bovine; Vanadium
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
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 Name: [5]
Energetix Corporation
Labeler Code:
64578
Product Label ID:
41234598-0cb5-41c2-bfbe-1c15ee9bf502
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
10-22-2014
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
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Code Structure Chart

Product Details

What is NDC 64578-0095?

The NDC code 64578-0095 is assigned by the FDA to the product Adaptopath which is a human over the counter drug product labeled by Energetix Corporation. The generic name of Adaptopath is adenosinum cyclophosphoricum, alpha-lipoicum acidum, argentum metallicum, avena sativa, capsicum annuum, citricum acidum, coenzyme a, cuprum metallicum, ginkgo biloba, glandula suprarenalis suis, glycyrrhiza glabra, hypothalamus (bovine), iodium, ledum palustre, manganum aceticum, nadidum, natrum carbonicum, oleum morrhuae, phosphoricum acidum, picricum acidum, riboflavinum, selenium metallicum sepia, silicea, thiaminum hydrochloricum, thyroidinum (bovine), vanadium metallicum. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 64578-0095-1 59.1 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are Adaptopath Active Ingredients?

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.
  • .ALPHA.-LIPOIC ACID 12 [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.
  • ADENOSINE CYCLIC PHOSPHATE 8 [hp_X]/mL
  • ANHYDROUS CITRIC ACID 4 [hp_X]/mL - A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.
  • AVENA SATIVA FLOWERING TOP 4 [hp_X]/mL
  • BOS TAURUS HYPOTHALAMUS 12 [hp_X]/mL
  • CAPSICUM 4 [hp_X]/mL - A plant genus of the family SOLANACEAE. The hot peppers yield CAPSAICIN, which activates VANILLOID RECEPTORS. Several varieties have sweet or pungent edible fruits that are used as vegetables when fresh and spices when the pods are dried.
  • COD LIVER OIL 6 [hp_X]/mL - Oil obtained from fresh livers of the cod family, Gadidae. It is a source of VITAMIN A and VITAMIN D.
  • COENZYME A 8 [hp_X]/mL - Venoms from jellyfish; CORALS; SEA ANEMONES; etc. They contain hemo-, cardio-, dermo- , and neuro-toxic substances and probably ENZYMES. They include palytoxin, sarcophine, and anthopleurine.
  • COPPER 12 [hp_X]/mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
  • GINKGO 4 [hp_X]/mL - The only specie of the genus Ginkgo, family Ginkgoacea. It is the source of extracts of medicinal interest, especially Egb 761. Ginkgo may refer to the genus or species.
  • GLYCYRRHIZA GLABRA 4 [hp_X]/mL - A genus of leguminous herbs or shrubs whose roots yield GLYCYRRHETINIC ACID and its derivative, CARBENOXOLONE.
  • IODINE 12 [hp_X]/mL - A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
  • LEDUM PALUSTRE TWIG 6 [hp_X]/mL
  • MANGANESE ACETATE TETRAHYDRATE 12 [hp_X]/mL
  • NADIDE 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • PICRIC ACID 12 [hp_X]/mL
  • RIBOFLAVIN 12 [hp_X]/mL - Nutritional factor found in milk, eggs, malted barley, liver, kidney, heart, and leafy vegetables. The richest natural source is yeast. It occurs in the free form only in the retina of the eye, in whey, and in urine; its principal forms in tissues and cells are as FLAVIN MONONUCLEOTIDE and FLAVIN-ADENINE DINUCLEOTIDE.
  • SELENIUM 12 [hp_X]/mL - An element with the atomic symbol Se, atomic number 34, and atomic weight 78.97. It is an essential micronutrient for mammals and other animals but is toxic in large amounts. Selenium protects intracellular structures against oxidative damage. It is an essential component of GLUTATHIONE PEROXIDASE.
  • SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
  • SILICON DIOXIDE 12 [hp_X]/mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
  • SILVER 12 [hp_X]/mL - An element with the atomic symbol Ag, atomic number 47, and atomic weight 107.87. It is a soft metal that is used medically in surgical instruments, dental prostheses, and alloys. Long-continued use of silver salts can lead to a form of poisoning known as ARGYRIA.
  • SODIUM CARBONATE 12 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 9 [hp_X]/mL
  • THIAMINE HYDROCHLORIDE 8 [hp_X]/mL
  • THYROID, BOVINE 9 [hp_X]/mL
  • VANADIUM 12 [hp_X]/mL - A metallic element with the atomic symbol V, atomic number 23, and atomic weight 50.94. It is used in the manufacture of vanadium steel. Prolonged exposure can lead to chronic intoxication caused by absorption usually via the lungs.

Which are Adaptopath UNII Codes?

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

Which are Adaptopath Inactive Ingredients 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 for Adaptopath?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

* Please review the disclaimer below.

Product Footnotes

[1] 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.

[2] 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.

[3] 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".