NDC 58264-0056 D56
Artemisia Cina Pre-flowering Top,Tanacetum Vulgare Whole,Artemisia Vulgaris - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58264 - Dna Labs, Inc.
- 58264-0056 - D56
Product Packages
NDC Code 58264-0056-1
Package Description: 29.57 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 58264-0056?
What are the uses for D56?
What are D56 Active Ingredients?
- ARTEMISIA CINA PRE-FLOWERING TOP 4 [hp_X]/mL
- ARTEMISIA VULGARIS WHOLE 1 [hp_X]/mL
- DRYOPTERIS FILIX-MAS ROOT 2 [hp_X]/mL
- GRAPHITE 30 [hp_X]/mL - 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.
- MERCURIC CHLORIDE 6 [hp_X]/mL - Mercury chloride (HgCl2). A highly toxic compound that volatizes slightly at ordinary temperature and appreciably at 100 degrees C. It is corrosive to mucous membranes and used as a topical antiseptic and disinfectant.
- TANACETUM VULGARE WHOLE 1 [hp_X]/mL
Which are D56 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARTEMISIA CINA PRE-FLOWERING TOP (UNII: 28M1820ACT)
- ARTEMISIA CINA PRE-FLOWERING TOP (UNII: 28M1820ACT) (Active Moiety)
- TANACETUM VULGARE WHOLE (UNII: CI1YT265BA)
- TANACETUM VULGARE WHOLE (UNII: CI1YT265BA) (Active Moiety)
- ARTEMISIA VULGARIS WHOLE (UNII: JDR81QW9ZQ)
- ARTEMISIA VULGARIS WHOLE (UNII: JDR81QW9ZQ) (Active Moiety)
- DRYOPTERIS FILIX-MAS ROOT (UNII: C0ZK0RRF5X)
- DRYOPTERIS FILIX-MAS ROOT (UNII: C0ZK0RRF5X) (Active Moiety)
- MERCURIC CHLORIDE (UNII: 53GH7MZT1R)
- MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
Which are D56 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)
* 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".