NDC 17089-463 Guna Arthro Relief
Arteria Suis - Alpha Ketoglutaricum Acidum - Alpha Lipoicum Acidum - Ascorbicum Acidum - - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 17089-463?
What are the uses for Guna Arthro Relief?
What are Guna Arthro Relief Active Ingredients?
- .ALPHA.-KETOGLUTARIC ACID 3 [hp_X]/30mL - A family of compounds containing an oxo group with the general structure of 1,5-pentanedioic acid. (From Lehninger, Principles of Biochemistry, 1982, p442)
- .ALPHA.-LIPOIC ACID 8 [hp_X]/30mL - An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS.
- ASCORBIC ACID 3 [hp_X]/30mL - 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.
- BARIUM OXALOSUCCINATE 6 [hp_X]/30mL
- BLACK COHOSH 6 [hp_X]/30mL
- BRYONIA ALBA ROOT 6 [hp_X]/30mL
- CHLORINE 6 [hp_X]/30mL - An element with atomic symbol Cl, atomic number 17, and atomic weight 35, and member of the halogen family.
- COLCHICUM AUTUMNALE BULB 6 [hp_X]/30mL
- NADIDE 3 [hp_X]/30mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 4 [hp_X]/30mL
- SODIUM DIETHYL OXALACETATE 3 [hp_X]/30mL
- SODIUM SULFATE 8 [hp_X]/30mL
- SOLANUM DULCAMARA FLOWER 6 [hp_X]/30mL
- SULFUR 4 [hp_X]/30mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
- SUS SCROFA ADRENAL GLAND 6 [hp_X]/30mL
- SUS SCROFA ARTERY 6 [hp_X]/30mL
- SUS SCROFA CARTILAGE 6 [hp_X]/30mL
- SUS SCROFA EMBRYO 6 [hp_X]/30mL
- SUS SCROFA PLACENTA 6 [hp_X]/30mL
- SUS SCROFA UMBILICAL CORD 6 [hp_X]/30mL
- SUS SCROFA VEIN 6 [hp_X]/30mL
- TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/30mL
Which are Guna Arthro Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- .ALPHA.-KETOGLUTARIC ACID (UNII: 8ID597Z82X)
- .ALPHA.-KETOGLUTARIC ACID (UNII: 8ID597Z82X) (Active Moiety)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y) (Active Moiety)
- SUS SCROFA ARTERY (UNII: 63O327782Q)
- SUS SCROFA ARTERY (UNII: 63O327782Q) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- BARIUM OXALOSUCCINATE (UNII: L7A49804ZQ)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F)
- SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F) (Active Moiety)
- CHLORINE (UNII: 4R7X1O2820)
- CHLORINE (UNII: 4R7X1O2820) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
- SUS SCROFA EMBRYO (UNII: 9928MC12VO)
- SUS SCROFA EMBRYO (UNII: 9928MC12VO) (Active Moiety)
- SOLANUM DULCAMARA FLOWER (UNII: W6J1279A6K)
- SOLANUM DULCAMARA FLOWER (UNII: W6J1279A6K) (Active Moiety)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- NADIDE (UNII: 0U46U6E8UK)
- NADIDE (UNII: 0U46U6E8UK) (Active Moiety)
- SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG)
- DIETHYL OXALACETATE (UNII: 15S56468G7) (Active Moiety)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- SUS SCROFA VEIN (UNII: 2510RH3I89)
- SUS SCROFA VEIN (UNII: 2510RH3I89) (Active Moiety)
Which are Guna Arthro Relief 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)
Which are the Pharmacologic Classes for Guna Arthro Relief?
- Ascorbic Acid - [CS]
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Vitamin C - [EPC] (Established Pharmacologic Class)
* 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".