NDC 63776-035 Arthros

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

NDC Product Code 63776-035

NDC CODE: 63776-035

Proprietary Name: Arthros What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: 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 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.

NDC Code Structure

NDC 63776-035-11

Package Description: .5 mL in 1 AMPULE

NDC 63776-035-14

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

NDC 63776-035-15

Package Description: 50 mL in 1 BOTTLE

NDC 63776-035-16

Package Description: 100 mL in 1 BOTTLE

NDC 63776-035-17

Package Description: 250 mL in 1 BOTTLE

NDC Product Information

Arthros with NDC 63776-035 is a 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.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug 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.

Arthros Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Viatrexx Bio Incorporated
Labeler Code: 63776
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 07-24-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Arthros Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Anti-Interleukin 1 (6X, 200K), Alpha Ketoglutaric Acid (6X, 30K), Alpha Lipoic Acid (6X, 30K), Apomorphine  (8X, 30K), Articulation capsule  (8X, 200K), Ascorbic acid  (8X, 30K), Adrenal  (8X, 200K), BDNF  (6X, 200K), Beta endorphin  (6X, 200K), bFGF  (6X, 200K), Coelliac plexus  (8X, 200K), Calcitonin  (8X, 200K), Cartilage  (6X, 200K), Colchicum automnale  (6C, 200K), Collagen  (8X, 200K), Erythrocytes  (8X, 200K), Interleukin-12  (6X, 200K), Interferon gamma  (6X, 200K), Liver  (6X, 200K), Lymph node  (8X, 200K), Mesenchyme  (6X, 200K), Nadid  (30K), Parathyroid  (6X, 200K), Placenta  (6X, 30K), Quinhydrone  (30K), Sulphur  (30K), Vein  (6X, 30K)

Purpose:

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

Uses

For the relief of arthritic symptoms

Warnings

Stop use and ask a health care practitioner if symptoms persist for more than five days or worsen. If pregnant or breastfeeding, ask a health care practitioner before use.

Dosage

1-3 spray(s); 1-3 time(s) per day or as recommended by your health care practitioner.

Inactive Ingredients

20% Alcohol and 80% Water

Other Information

Normal storage use.Do not use if tamper-evident seal is broken or removed.

Questions

[email protected]

* Please review the disclaimer below.