NDC 63479-0307 C07 Strong Ligaments And Joints
Arnica Montana,Ascorbicum Acidum,Bos Taurus Lymph Vessel,Intervertebral Fibrocartilage,Bos - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63479 - Apex Energetics Inc.
- 63479-0307 - C07
Product Packages
NDC Code 63479-0307-1
Package Description: 30 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 63479-0307?
What are the uses for C07 Strong Ligaments And Joints?
What are C07 Strong Ligaments And Joints Active Ingredients?
- ARNICA MONTANA 12 [hp_X]/mL
- ASCORBIC ACID 8 [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.
- BOS TAURUS INTERVERTEBRAL DISC 8 [hp_C]/mL
- BOS TAURUS LYMPH VESSEL 7 [hp_C]/mL
- BOS TAURUS MESENCHYME 8 [hp_C]/mL
- CALCIUM HEXAFLUOROSILICATE 12 [hp_X]/mL
- COMFREY ROOT 9 [hp_X]/mL
- FORMIC ACID 12 [hp_X]/mL
- FRANGULA CALIFORNICA BARK 8 [hp_X]/mL
- PINUS MUGO LEAFY TWIG 7 [hp_X]/mL
- RUTA GRAVEOLENS FLOWERING TOP 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.
- SUS SCROFA CARTILAGE 7 [hp_C]/mL
- SUS SCROFA JOINT CAPSULE 8 [hp_C]/mL
- SUS SCROFA LIGAMENT 8 [hp_C]/mL
- SUS SCROFA MENISCUS 7 [hp_C]/mL
- SUS SCROFA PARATHYROID GLAND 8 [hp_C]/mL
- SUS SCROFA VEIN 7 [hp_C]/mL
- TOXICODENDRON PUBESCENS LEAF 15 [hp_X]/mL
- TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/mL
Which are C07 Strong Ligaments And Joints UNII Codes?
The UNII codes for the active ingredients in this product are:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SUS SCROFA LIGAMENT (UNII: 2004Q810JO)
- SUS SCROFA LIGAMENT (UNII: 2004Q810JO) (Active Moiety)
- SUS SCROFA MENISCUS (UNII: 1C8T78BD9Q)
- SUS SCROFA MENISCUS (UNII: 1C8T78BD9Q) (Active Moiety)
- SUS SCROFA PARATHYROID GLAND (UNII: 2KBE35NE8S)
- SUS SCROFA PARATHYROID GLAND (UNII: 2KBE35NE8S) (Active Moiety)
- SUS SCROFA VEIN (UNII: 2510RH3I89)
- SUS SCROFA VEIN (UNII: 2510RH3I89) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- BOS TAURUS MESENCHYME (UNII: 3802H34QRI)
- BOS TAURUS MESENCHYME (UNII: 3802H34QRI) (Active Moiety)
- BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV)
- BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV) (Active Moiety)
- BOS TAURUS INTERVERTEBRAL DISC (UNII: 0A04Z76C13)
- BOS TAURUS INTERVERTEBRAL DISC (UNII: 0A04Z76C13) (Active Moiety)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F)
- SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F) (Active Moiety)
- FORMIC ACID (UNII: 0YIW783RG1)
- FORMIC ACID (UNII: 0YIW783RG1) (Active Moiety)
- CALCIUM HEXAFLUOROSILICATE (UNII: 2NVP93XVQ3)
- CALCIUM HEXAFLUOROSILICATE (UNII: 2NVP93XVQ3) (Active Moiety)
- PINUS MUGO LEAFY TWIG (UNII: 787BZ3D14H)
- PINUS MUGO LEAFY TWIG (UNII: 787BZ3D14H) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- SUS SCROFA JOINT CAPSULE (UNII: LX0XHE5NLN)
- SUS SCROFA JOINT CAPSULE (UNII: LX0XHE5NLN) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- FRANGULA CALIFORNICA BARK (UNII: 1LZ13MQR0S)
- FRANGULA CALIFORNICA BARK (UNII: 1LZ13MQR0S) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
Which are C07 Strong Ligaments And Joints 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for C07 Strong Ligaments And Joints?
* 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".