NDC 63479-0304 C04 Arthro Muscotox
Actaea Spicata,Ammonium Benzoicum,Arnica Montana,Bellis Perennis,Berberis - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 63479-0304?
What are the uses for C04 Arthro Muscotox?
What are C04 Arthro Muscotox Active Ingredients?
- ACTAEA SPICATA ROOT 12 [hp_X]/mL
- AMMONIUM BENZOATE 9 [hp_X]/mL
- ARNICA MONTANA 30 [hp_X]/mL
- BELLIS PERENNIS 12 [hp_X]/mL
- BERBERIS VULGARIS ROOT BARK 1 [hp_X]/mL
- BRYONIA ALBA ROOT 30 [hp_X]/mL
- CHELIDONIUM MAJUS 1 [hp_X]/mL - A plant species of the family PAPAVERACEAE. The common name greater celandine is similar to lesser celandine (Ficaria verna), and celandine poppy (Stylophorum diphyllum). It has been used in folk medicine and its latex contains biologically active compounds including BENZOPHENANTHRIDINES alkaloids (e.g., Chelerythrine).
- COMFREY ROOT 9 [hp_X]/mL
- ECHINACEA PURPUREA 1 [hp_X]/mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- FORMICA RUFA 30 [hp_X]/mL
- FRAXINUS EXCELSIOR LEAF 1 [hp_X]/mL
- LACTIC ACID, DL- 30 [hp_X]/mL
- LACTIC ACID, L- 15 [hp_X]/mL
- PULSATILLA VULGARIS WHOLE 30 [hp_X]/mL
- QUININE SULFATE 9 [hp_X]/mL - An alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood.
- RHODODENDRON AUREUM LEAF 12 [hp_X]/mL
- RHODODENDRON TOMENTOSUM LEAFY TWIG 6 [hp_X]/mL
- RUTA GRAVEOLENS FLOWERING TOP 9 [hp_X]/mL
- SOLANUM DULCAMARA WHOLE 30 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 30 [hp_X]/mL
- URIC ACID 15 [hp_X]/mL - An oxidation product, via XANTHINE OXIDASE, of oxypurines such as XANTHINE and HYPOXANTHINE. It is the final oxidation product of purine catabolism in humans and primates, whereas in most other mammals URATE OXIDASE further oxidizes it to ALLANTOIN.
Which are C04 Arthro Muscotox UNII Codes?
The UNII codes for the active ingredients in this product are:
- SOLANUM DULCAMARA WHOLE (UNII: G72JA9DHK5)
- SOLANUM DULCAMARA WHOLE (UNII: G72JA9DHK5) (Active Moiety)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- ACTAEA SPICATA ROOT (UNII: 3FU86L9OS0)
- ACTAEA SPICATA ROOT (UNII: 3FU86L9OS0) (Active Moiety)
- FORMICA RUFA (UNII: 55H0W83JO5)
- FORMICA RUFA (UNII: 55H0W83JO5) (Active Moiety)
- FRAXINUS EXCELSIOR LEAF (UNII: RC38362Q7M)
- FRAXINUS EXCELSIOR LEAF (UNII: RC38362Q7M) (Active Moiety)
- LACTIC ACID, DL- (UNII: 3B8D35Y7S4)
- LACTIC ACID, DL- (UNII: 3B8D35Y7S4) (Active Moiety)
- RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U)
- RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- PULSATILLA VULGARIS WHOLE (UNII: I76KB35JEV)
- PULSATILLA VULGARIS WHOLE (UNII: I76KB35JEV) (Active Moiety)
- RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P)
- RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P) (Active Moiety)
- AMMONIUM BENZOATE (UNII: AC80WD7GPF)
- AMMONIUM BENZOATE (UNII: AC80WD7GPF) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- LACTIC ACID, L- (UNII: F9S9FFU82N)
- LACTIC ACID, L- (UNII: F9S9FFU82N) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- URIC ACID (UNII: 268B43MJ25)
- URIC ACID (UNII: 268B43MJ25) (Active Moiety)
- BELLIS PERENNIS (UNII: 2HU33I03UY)
- BELLIS PERENNIS (UNII: 2HU33I03UY) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- QUININE SULFATE (UNII: KF7Z0E0Q2B)
- QUININE (UNII: A7V27PHC7A) (Active Moiety)
Which are C04 Arthro Muscotox 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes for C04 Arthro Muscotox?
* Please review the disclaimer below.
[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".