NDC 44911-0684 Vermistat
Artemisia Vulgaris,Cina,Sabadilla,Spigelia Anthelmia,Filix Mas,Baryta Carbonica,Calcarea - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 44911-0684?
What are the uses for Vermistat?
What are Vermistat Active Ingredients?
- ARTEMISIA CINA PRE-FLOWERING TOP 3 [hp_X]/mL
- ARTEMISIA VULGARIS ROOT 3 [hp_X]/mL
- BARIUM CARBONATE 12 [hp_X]/mL
- CINCHONA OFFICINALIS BARK 12 [hp_X]/mL
- DRYOPTERIS FILIX-MAS ROOT 4 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
- PROTEUS VULGARIS 30 [hp_X]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that occurs in soil, fecal matter, and sewage. It is an opportunistic pathogen and causes cystitis and pyelonephritis.
- SCHOENOCAULON OFFICINALE SEED 3 [hp_X]/mL
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 12 [hp_X]/mL
- SPIGELIA ANTHELMIA WHOLE 3 [hp_X]/mL
- SULFUR 12 [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.
- TURPENTINE OIL 12 [hp_X]/mL
Which are Vermistat UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S) (Active Moiety)
- ARTEMISIA CINA PRE-FLOWERING TOP (UNII: 28M1820ACT)
- ARTEMISIA CINA FLOWER (UNII: 28M1820ACT) (Active Moiety)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
- SPIGELIA ANTHELMIA WHOLE (UNII: WYT05213GE)
- SPIGELIA ANTHELMIA (UNII: WYT05213GE) (Active Moiety)
- DRYOPTERIS FILIX-MAS ROOT (UNII: C0ZK0RRF5X)
- DRYOPTERIS FILIX-MAS ROOT (UNII: C0ZK0RRF5X) (Active Moiety)
- BARIUM CARBONATE (UNII: 6P669D8HQ8)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- TURPENTINE OIL (UNII: C5H0QJ6V7F)
- TURPENTINE OIL (UNII: C5H0QJ6V7F) (Active Moiety)
- PROTEUS VULGARIS (UNII: 11T9HCO30O)
- PROTEUS VULGARIS (UNII: 11T9HCO30O) (Active Moiety)
Which are Vermistat 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)
* 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".