NDC 43742-1273 Chronagesic
Arnica Montana,Cinnamomum,Dulcamara,Funiculus Umbilicalis Suis,Nadidum,Natrum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43742-1273?
What are the uses for Chronagesic?
What are Chronagesic Active Ingredients?
- .ALPHA.-LIPOIC ACID 8 [hp_X]/mL - 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.
- APIOLE (PARSLEY) 6 [hp_X]/mL
- ARNICA MONTANA 3 [hp_X]/mL
- CINNAMON 6 [hp_X]/mL
- COMFREY ROOT 8 [hp_X]/mL
- GREEN PEPPERCORN 6 [hp_X]/mL
- NADIDE 6 [hp_X]/mL
- PANTOTHENIC ACID 6 [hp_X]/mL - A butyryl-beta-alanine that can also be viewed as pantoic acid complexed with BETA ALANINE. It is incorporated into COENZYME A and protects cells against peroxidative damage by increasing the level of GLUTATHIONE.
- SANGUINARIA CANADENSIS ROOT 6 [hp_X]/mL
- SILICON DIOXIDE 8 [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.
- SODIUM DIETHYL OXALACETATE 6 [hp_X]/mL
- SOLANUM DULCAMARA TOP 6 [hp_X]/mL
- SULFUR 6 [hp_X]/mL - 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 CARTILAGE 8 [hp_X]/mL
- SUS SCROFA PLACENTA 6 [hp_X]/mL
- SUS SCROFA UMBILICAL CORD 6 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 8 [hp_X]/mL
Which are Chronagesic UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- CINNAMON (UNII: 5S29HWU6QB)
- CINNAMON (UNII: 5S29HWU6QB) (Active Moiety)
- SOLANUM DULCAMARA TOP (UNII: KPS1B1162N)
- SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (Active Moiety)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H) (Active Moiety)
- NADIDE (UNII: 0U46U6E8UK)
- NADIDE (UNII: 0U46U6E8UK) (Active Moiety)
- SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG)
- DIETHYL OXALACETATE (UNII: 15S56468G7) (Active Moiety)
- PANTOTHENIC ACID (UNII: 19F5HK2737)
- PANTOTHENIC ACID (UNII: 19F5HK2737) (Active Moiety)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8) (Active Moiety)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- APIOLE (PARSLEY) (UNII: QQ67504PXO)
- APIOLE (PARSLEY) (UNII: QQ67504PXO) (Active Moiety)
- GREEN PEPPERCORN (UNII: 6G53L8ESRK)
- GREEN PEPPERCORN (UNII: 6G53L8ESRK) (Active Moiety)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y) (Active Moiety)
- SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F)
- SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
Which are Chronagesic 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 Chronagesic?
* 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.
[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
[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".