Adaptagen Liquid
NDC 43857-0506

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43857-0506?
  4. Adaptagen Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Adaptagen (aralia quinquefolia, avena sativa, capsicum annuum, ginkgo biloba, glycyrrhiza glabra, hydrocotyle asiatica, thiaminum hydrochloricum, ascorbicum acidum, riboflavinum, glandula suprarenalis suis, spleen (suis), thyroidinum (suis), cuprum gluconate, iodium, ledum palustre, molybdenum metallicum, natrum carbonicum, phosphoricum acidum, picricum acidum, selenium metallicum, sepia, vanadium metallicum, adenosinum triphosphoricum dinatrum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Bioactive Nutritional, 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 43857-0506 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43857-0506
Proprietary Name:
Adaptagen
Non-Proprietary Name: [1]
Aralia Quinquefolia, Avena Sativa, Capsicum Annuum, Ginkgo Biloba, Glycyrrhiza Glabra, Hydrocotyle Asiatica, Thiaminum Hydrochloricum, Ascorbicum Acidum, Riboflavinum, Glandula Suprarenalis Suis, Spleen (suis), Thyroidinum (suis), Cuprum Gluconate, Iodium, Ledum Palustre, Molybdenum Metallicum, Natrum Carbonicum, Phosphoricum Acidum, Picricum Acidum, Selenium Metallicum, Sepia, Vanadium Metallicum, Adenosinum Triphosphoricum Dinatrum
Substance Name: [2]
Adenosine Triphosphate Disodium; American Ginseng; Ascorbic Acid; Avena Sativa Flowering Top; Capsicum; Centella Asiatica; Copper Gluconate; Ginkgo; Glycyrrhiza Glabra; Iodine; Ledum Palustre Twig; Molybdenum; Phosphoric Acid; Picric Acid; Riboflavin; Selenium; Sepia Officinalis Juice; Sodium Carbonate; Sus Scrofa Adrenal Gland; Sus Scrofa Spleen; Sus Scrofa Thyroid; Thiamine Hydrochloride; Vanadium
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]
Bioactive Nutritional, Inc.
Labeler Code:
43857
Product Label ID:
9404d71c-8a2e-4e68-bf48-8536bb14fc88
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
02-08-2019
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43857-0506?

The NDC code 43857-0506 is assigned by the FDA to the product Adaptagen. It is commonly known by its generic name, aralia quinquefolia, avena sativa, capsicum annuum, ginkgo biloba, glycyrrhiza glabra, hydrocotyle asiatica, thiaminum hydrochloricum, ascorbicum acidum, riboflavinum, glandula suprarenalis suis, spleen (suis), thyroidinum (suis), cuprum gluconate, iodium, ledum palustre, molybdenum metallicum, natrum carbonicum, phosphoricum acidum, picricum acidum, selenium metallicum, sepia, vanadium metallicum, adenosinum triphosphoricum dinatrum. This pharmaceutical product is labeled by Bioactive Nutritional, 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: 43857-0506-1. 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 temporary relief of tiredness, weakness, general fatigue, exhaustion, and weakness of memory. For temporary relief of tiredness, weakness, general fatigue, exhaustion, and weakness of memory.

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.
  • ADENOSINE TRIPHOSPHATE DISODIUM 30 [hp_X]/mL
  • AMERICAN GINSENG 3 [hp_X]/mL
  • ASCORBIC ACID 6 [hp_X]/mL - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
  • AVENA SATIVA FLOWERING TOP 3 [hp_X]/mL
  • CAPSICUM 3 [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.
  • CENTELLA ASIATICA 3 [hp_X]/mL - A plant of the family APIACEAE which is the source of asiatic acid and asiaticoside. Centella asiatica (L.) Urb. = Hydrocotyle asiatica L. is known for effect on peripheral circulation.
  • COPPER GLUCONATE 12 [hp_X]/mL - Derivatives of gluconic acid (the structural formula HOCH2(CHOH)4COOH), including its salts and esters.
  • GINKGO 3 [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 3 [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 12 [hp_X]/mL
  • MOLYBDENUM 12 [hp_X]/mL - A metallic element with the atomic symbol Mo, atomic number 42, and atomic weight 95.95. It is an essential trace element, being a component of the enzymes xanthine oxidase, aldehyde oxidase, and nitrate reductase.
  • PHOSPHORIC ACID 12 [hp_X]/mL - Inorganic derivatives of phosphoric acid (H3PO4). Note that organic derivatives of phosphoric acids are listed under ORGANOPHOSPHATES.
  • PICRIC ACID 12 [hp_X]/mL - used as antiseptic, astringent & stimulant for epitheliazation; structure
  • RIBOFLAVIN 6 [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
  • SODIUM CARBONATE 12 [hp_X]/mL - used topically for dermatitides, mouthwash, vaginal douche; veterinary use as emergency emetic; RN given refers to carbonic acid, di-Na salt; structure
  • SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
  • SUS SCROFA SPLEEN 8 [hp_X]/mL
  • SUS SCROFA THYROID 8 [hp_X]/mL
  • THIAMINE HYDROCHLORIDE 4 [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 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:

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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".