NDC 63776-035 Arthros

Anti-interleukin-1.alpha. Immunoglobulin G Rabbit,.alpha.-ketoglutaric Acid,.alpha.-lipoic - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
63776-035
Proprietary Name:
Arthros
Non-Proprietary Name: [1]
Anti-interleukin-1.alpha. Immunoglobulin G Rabbit, .alpha.-ketoglutaric Acid, .alpha.-lipoic Acid, Apomorphine, Bos Taurus Joint Capsule, Sus Scrofa Joint Capsule, Ascorbic Acid, Bos Taurus Adrenal Gland, Sus Scrofa Adrenal Gland, Brain-derived Neurotrophic Factor Human, Metenkefalin, Ersofermin, Bos Taurus Solar Plexus, Sus Scrofa Solar Plexus, Calcitonin, Bos Taurus Cartilage, Sus Scrofa Cartilage, Colchicum Autumnale Bulb, Pork Collagen, Bos Taurus Red Blood Cell, Sus Scrofa Red Blood Cell
Substance Name: [2]
.alpha.-ketoglutaric Acid; .alpha.-lipoic Acid; Anti-interleukin-1.alpha. Immunoglobulin G Rabbit; Apomorphine; Ascorbic Acid; Beef Liver; Bos Taurus Adrenal Gland; Bos Taurus Cartilage; Bos Taurus Joint Capsule; Bos Taurus Lymph; Bos Taurus Mesenchyme; Bos Taurus Parathyroid Gland; Bos Taurus Placenta; Bos Taurus Red Blood Cell; Bos Taurus Solar Plexus; Bos Taurus Vein; Brain-derived Neurotrophic Factor Human; Calcitonin; Colchicum Autumnale Bulb; Edodekin Alfa; Ersofermin; Interferon Gamma-1a; Metenkefalin; Nadide; Pork Collagen; Pork Liver; Quinhydrone; Sulfur; Sus Scrofa Adrenal Gland; Sus Scrofa Cartilage; Sus Scrofa Joint Capsule; Sus Scrofa Lymph; Sus Scrofa Mesenchyme; Sus Scrofa Parathyroid Gland; Sus Scrofa Red Blood Cell; Sus Scrofa Solar Plexus; Sus Scrofa Vein
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Viatrexx Bio Incorporated
    Labeler Code:
    63776
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    07-24-2012
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 63776-035-14

    Package Description: 1 BOTTLE, SPRAY in 1 BOX / 30 mL in 1 BOTTLE, SPRAY

    Product Details

    What is NDC 63776-035?

    The NDC code 63776-035 is assigned by the FDA to the product Arthros which is a human over the counter drug product labeled by Viatrexx Bio Incorporated. The generic name of Arthros is anti-interleukin-1.alpha. immunoglobulin g rabbit, .alpha.-ketoglutaric acid, .alpha.-lipoic acid, apomorphine, bos taurus joint capsule, sus scrofa joint capsule, ascorbic acid, bos taurus adrenal gland, sus scrofa adrenal gland, brain-derived neurotrophic factor human, metenkefalin, ersofermin, bos taurus solar plexus, sus scrofa solar plexus, calcitonin, bos taurus cartilage, sus scrofa cartilage, colchicum autumnale bulb, pork collagen, bos taurus red blood cell, sus scrofa red blood cell. The product's dosage form is spray and is administered via oral form. The product is distributed in a single package with assigned NDC code 63776-035-14 1 bottle, spray in 1 box / 30 ml in 1 bottle, spray. 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 the uses for Arthros?

    This product is used as Anti-Interleukin 1Anti-inflammation Alpha Ketoglutaric Acid Cell respirationAlpha Lipoic Acid Anti-agingApomorphine Pain relief Articulation capsule RegenerationAscorbic acid Anti-oxidantAdrenalAdrenal supportBDNFRegenerationBeta endorphin Pain reliefbFGFRegenerationCoelliac plexus Neurological supportCalcitoninCalcium balance CartilageRegenerationColchicum automnaleDrainageCollagenRegenerationErythrocytesImmune supportInterleukin-12 Immune supportInterferon gamma Immune supportLiverDrainage Lymph node Immune supportMesenchymeRegenerationNadidCell respirationParathyroidRegenerationPlacentaRegenerationQuinhydroneCitric cycle supportSulphurDrainageVeinRegeneration. For the relief of arthritic symptoms

    What are Arthros 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.

    Which are Arthros UNII Codes?

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

    Which are Arthros 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 Arthros?

    * 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".