NDC 62106-1194 Drosera Plex
Arnica Montana,Belladonna,Cina,Coccus Cacti,Corallium Rubrum,Cuprum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 62106-1194?
What are the uses for Drosera Plex?
What are Drosera Plex Active Ingredients?
- ARNICA MONTANA ROOT 6 [hp_X]/30mL
- ARTEMISIA CINA FLOWER 6 [hp_X]/30mL
- ATROPA BELLADONNA WHOLE 6 [hp_X]/30mL
- COPPER 6 [hp_X]/30mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
- CORALLIUM RUBRUM EXOSKELETON 6 [hp_X]/30mL
- DROSERA ROTUNDIFOLIA FLOWERING TOP 6 [hp_X]/30mL
- FERRUM PHOSPHORICUM 6 [hp_X]/30mL
- IPECAC 6 [hp_X]/30mL - A syrup made from the dried rhizomes of two different species, CEPHAELIS ipecacuanha and C. acuminata. They contain EMETINE, cephaeline, psychotrine and other ISOQUINOLINES. Ipecac syrup is used widely as an emetic acting both locally on the gastric mucosa and centrally on the chemoreceptor trigger zone.
- PROTORTONIA CACTI 6 [hp_X]/30mL
- SOLIDAGO VIRGAUREA FLOWERING TOP 2 [hp_X]/30mL
Which are Drosera Plex UNII Codes?
The UNII codes for the active ingredients in this product are:
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- ARTEMISIA CINA FLOWER (UNII: 28M1820ACT)
- ARTEMISIA CINA FLOWER (UNII: 28M1820ACT) (Active Moiety)
- FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7)
- FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7) (Active Moiety)
- IPECAC (UNII: 62I3C8233L)
- IPECAC (UNII: 62I3C8233L) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
- DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG)
- DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG) (Active Moiety)
- ATROPA BELLADONNA WHOLE (UNII: DSV74G1P2J)
- ATROPA BELLADONNA WHOLE (UNII: DSV74G1P2J) (Active Moiety)
- ARNICA MONTANA ROOT (UNII: MUE8Y11327)
- ARNICA MONTANA ROOT (UNII: MUE8Y11327) (Active Moiety)
- PROTORTONIA CACTI (UNII: LZB7TFX1LT)
- PROTORTONIA CACTI (UNII: LZB7TFX1LT) (Active Moiety)
- CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE)
- CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE) (Active Moiety)
Which are Drosera Plex 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)
Which are the Pharmacologic Classes for Drosera Plex?
* 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".