NDC 64578-0073 Para-chord
Homeopathic Liquid Liquid Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 64578-0073?
What are Para-chord Active Ingredients?
- ARTEMISIA ABROTANUM FLOWERING TOP 12 [hp_X]/59.1mL
- ARTEMISIA CINA PRE-FLOWERING TOP 5 [hp_X]/59.1mL
- ARTEMISIA VULGARIS ROOT 12 [hp_X]/59.1mL
- DRYOPTERIS FILIX-MAS ROOT 4 [hp_X]/59.1mL
- DYSPHANIA AMBROSIOIDES 12 [hp_X]/59.1mL
- GRAPHITE 12 [hp_X]/59.1mL - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 15 [hp_X]/59.1mL
- PEUMUS BOLDUS LEAF 4 [hp_X]/59.1mL
- PUNICA GRANATUM ROOT BARK 12 [hp_X]/59.1mL
- SILICON DIOXIDE 12 [hp_X]/59.1mL - 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 PHOSPHATE, DIBASIC 12 [hp_X]/59.1mL
- SPIGELIA ANTHELMIA 6 [hp_C]/59.1mL
- TANACETUM VULGARE TOP 12 [hp_X]/59.1mL
- TEUCRIUM MARUM 5 [hp_X]/59.1mL
- WHITE MUSTARD SEED 12 [hp_X]/59.1mL
Which are Para-chord UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0)
- ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0) (Active Moiety)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S) (Active Moiety)
- PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O)
- PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- DYSPHANIA AMBROSIOIDES (UNII: 4H5RSU087I)
- DYSPHANIA AMBROSIOIDES (UNII: 4H5RSU087I) (Active Moiety)
- ARTEMISIA CINA PRE-FLOWERING TOP (UNII: 28M1820ACT)
- ARTEMISIA CINA PRE-FLOWERING TOP (UNII: 28M1820ACT) (Active Moiety)
- DRYOPTERIS FILIX-MAS ROOT (UNII: C0ZK0RRF5X)
- DRYOPTERIS FILIX-MAS ROOT (UNII: C0ZK0RRF5X) (Active Moiety)
- PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D)
- PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- WHITE MUSTARD SEED (UNII: 25VR943RPP)
- WHITE MUSTARD SEED (UNII: 25VR943RPP) (Active Moiety)
- SPIGELIA ANTHELMIA (UNII: WYT05213GE)
- SPIGELIA ANTHELMIA (UNII: WYT05213GE) (Active Moiety)
- TANACETUM VULGARE TOP (UNII: D52957JQ8M)
- TANACETUM VULGARE TOP (UNII: D52957JQ8M) (Active Moiety)
- TEUCRIUM MARUM (UNII: 10464S0TAA)
- TEUCRIUM MARUM (UNII: 10464S0TAA) (Active Moiety)
Which are Para-chord 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALCOHOL (UNII: 3K9958V90M)
* 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".