NDC 44911-0523 Organdrainex
Allium Cepa,Allium Sativum,Ambrosia Artemisiaefolia,Berberis Vulgaris,Chelidonium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 44911 - Energique, Inc.
- 44911-0523 - Organdrainex
Product Packages
NDC Code 44911-0523-1
Package Description: 118 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 44911-0523?
What are the uses for Organdrainex?
What are Organdrainex Active Ingredients?
- ALOE 6 [hp_X]/mL - A plant genus of the family ASPHODELACEAE which is used medicinally. It contains anthraquinone glycosides such as aloin-emodin or aloe-emodin (EMODIN).
- ALPHA LIPOIC ACID 12 [hp_X]/mL - An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS.
- AMBROSIA ARTEMISIIFOLIA WHOLE 3 [hp_X]/mL
- BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
- CHELIDONIUM MAJUS WHOLE 3 [hp_X]/mL
- COLLINSONIA CANADENSIS ROOT 3 [hp_X]/mL
- CYNARA SCOLYMUS LEAF 3 [hp_X]/mL
- GARLIC 3 [hp_X]/mL - 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.
- METHYLCOBALAMIN 4 [hp_X]/mL
- ONION 3 [hp_X]/mL - Herbaceous biennial plants and their edible bulbs, belonging to the Allium genus.
- PALLADIUM 12 [hp_X]/mL - A chemical element having an atomic weight of 106.4, atomic number of 46, and the symbol Pd. It is a white, ductile metal resembling platinum, and following it in abundance and importance of applications. It is used in dentistry in the form of gold, silver, and copper alloys.
- PETROSELINUM CRISPUM WHOLE 3 [hp_X]/mL
- TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
Which are Organdrainex UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- GARLIC (UNII: V1V998DC17)
- GARLIC (UNII: V1V998DC17) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA WHOLE (UNII: 9W34L2CQ9A)
- AMBROSIA ARTEMISIIFOLIA WHOLE (UNII: 9W34L2CQ9A) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN) (Active Moiety)
- COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR)
- COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (Active Moiety)
- CYNARA SCOLYMUS LEAF (UNII: B71UA545DE)
- CYNARA SCOLYMUS LEAF (UNII: B71UA545DE) (Active Moiety)
- PETROSELINUM CRISPUM WHOLE (UNII: 1WZA4Y92EX)
- PETROSELINUM CRISPUM WHOLE (UNII: 1WZA4Y92EX) (Active Moiety)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (Active Moiety)
- METHYLCOBALAMIN (UNII: BR1SN1JS2W)
- METHYLCOBALAMIN (UNII: BR1SN1JS2W) (Active Moiety)
- ALOE (UNII: V5VD430YW9)
- ALOE (UNII: V5VD430YW9) (Active Moiety)
- ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y)
- ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y) (Active Moiety)
- PALLADIUM (UNII: 5TWQ1V240M)
- PALLADIUM (UNII: 5TWQ1V240M) (Active Moiety)
Which are Organdrainex 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Organdrainex?
* 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.
[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
[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".