NDC 59469-320 Mucan
Amanita Muscaria Fruiting Body,Garlic,Aristolochia Clematitis Whole,Simaba Cedron - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59469 - Pekana Naturheilmittel Gmbh
- 59469-320 - Mucan
Product Packages
NDC Code 59469-320-10
Package Description: 1 BOTTLE, GLASS in 1 BOX / 50 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 59469-320?
What are the uses for Mucan?
What are Mucan Active Ingredients?
- AMANITA MUSCARIA FRUITING BODY 6 [hp_X]/50mL
- ARISTOLOCHIA CLEMATITIS WHOLE 12 [hp_X]/50mL
- GARLIC 6 [hp_X]/50mL - A species of Allium used as a spice (SPICES) and traditional remedy. It contains alliin lyase and alliin, which is converted by alliin lyase to allicin, the pungent ingredient responsible for the aroma of fresh cut garlic.
- GOLDENSEAL 12 [hp_X]/50mL
- HOMALOLEPIS CEDRON SEED 6 [hp_X]/50mL
- OKOUBAKA AUBREVILLEI BARK 6 [hp_X]/50mL
- VINCETOXICUM HIRUNDINARIA LEAF 5 [hp_X]/50mL
Which are Mucan UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037)
- AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037) (Active Moiety)
- GARLIC (UNII: V1V998DC17)
- GARLIC (UNII: V1V998DC17) (Active Moiety)
- ARISTOLOCHIA CLEMATITIS WHOLE (UNII: T47L342B3C)
- ARISTOLOCHIA CLEMATITIS WHOLE (UNII: T47L342B3C) (Active Moiety)
- SIMABA CEDRON SEED (UNII: KHI40967MV)
- SIMABA CEDRON SEED (UNII: KHI40967MV) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- OKOUBAKA AUBREVILLEI BARK (UNII: MK2074187Z)
- OKOUBAKA AUBREVILLEI BARK (UNII: MK2074187Z) (Active Moiety)
- VINCETOXICUM HIRUNDINARIA LEAF (UNII: 9WLP0FA6U4)
- VINCETOXICUM HIRUNDINARIA LEAF (UNII: 9WLP0FA6U4) (Active Moiety)
Which are Mucan 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 Mucan?
* 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".