NDC 43742-1564 Kidney Drainage
Solidago Virgaurea,Asparagus Officinalis,Juniperus Communis,Sabal - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43742-1564?
What are the uses for Kidney Drainage?
What are Kidney Drainage Active Ingredients?
- ARCTOSTAPHYLOS UVA-URSI LEAF 2 [hp_X]/mL
- ASPARAGUS 2 [hp_X]/mL
- BENZOIC ACID 12 [hp_X]/mL - A fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid.
- BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
- CALCIUM SULFIDE 8 [hp_X]/mL
- COBALT 16 [hp_X]/mL - A trace element that is a component of vitamin B12. It has the atomic symbol Co, atomic number 27, and atomic weight 58.93. It is used in nuclear weapons, alloys, and pigments. Deficiency in animals leads to anemia; its excess in humans can lead to erythrocytosis.
- DELPHINIUM STAPHISAGRIA SEED 6 [hp_X]/mL
- EQUISETUM ARVENSE TOP 3 [hp_X]/mL
- FAGUS SYLVATICA FLOWERING TOP 8 [hp_X]/mL
- JUNIPERUS COMMUNIS WHOLE 2 [hp_X]/mL
- LARIX DECIDUA FLOWERING TOP 8 [hp_X]/mL
- LYTTA VESICATORIA 8 [hp_X]/mL
- MANGANESE 8 [hp_X]/mL - A trace element with atomic symbol Mn, atomic number 25, and atomic weight 54.94. It is concentrated in cell mitochondria, mostly in the pituitary gland, liver, pancreas, kidney, and bone, influences the synthesis of mucopolysaccharides, stimulates hepatic synthesis of cholesterol and fatty acids, and is a cofactor in many enzymes, including arginase and alkaline phosphatase in the liver. (From AMA Drug Evaluations Annual 1992, p2035)
- MIMULUS GUTTATUS FLOWERING TOP 8 [hp_X]/mL
- NITRIC ACID 8 [hp_X]/mL - Nitric acid (HNO3). A colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals. Continued exposure to vapor may cause chronic bronchitis; chemical pneumonitis may occur. (From Merck Index, 11th ed)
- PORK KIDNEY 8 [hp_X]/mL
- RHUS AROMATICA ROOT BARK 8 [hp_X]/mL
- RUBIA TINCTORUM ROOT 6 [hp_X]/mL
- SAW PALMETTO 2 [hp_X]/mL
- SILICON DIOXIDE 8 [hp_X]/mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
- SOLIDAGO VIRGAUREA FLOWERING TOP 1 [hp_X]/mL
- SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
- ULEX EUROPAEUS FLOWER 8 [hp_X]/mL
- URTICA DIOICA 3 [hp_X]/mL - A plant species of the genus Urtica, family URTICACEAE. Roots have been used to treat PROSTATIC HYPERPLASIA. Leaves are edible after the stinging quality is eliminated by brief heating.
Which are Kidney Drainage UNII Codes?
The UNII codes for the active ingredients in this product are:
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
- ASPARAGUS (UNII: Z1EJP3037Z)
- ASPARAGUS (UNII: Z1EJP3037Z) (Active Moiety)
- JUNIPERUS COMMUNIS WHOLE (UNII: 464910T5N9)
- JUNIPERUS COMMUNIS WHOLE (UNII: 464910T5N9) (Active Moiety)
- SAW PALMETTO (UNII: J7WWH9M8QS)
- SAW PALMETTO (UNII: J7WWH9M8QS) (Active Moiety)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (Active Moiety)
- URTICA DIOICA (UNII: 710FLW4U46)
- URTICA DIOICA (UNII: 710FLW4U46) (Active Moiety)
- RUBIA TINCTORUM ROOT (UNII: 0SVP95L23G)
- RUBIA TINCTORUM ROOT (UNII: 0SVP95L23G) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT) (Active Moiety)
- FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U)
- FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- PORK KIDNEY (UNII: X7BCI5P86H)
- PORK KIDNEY (UNII: X7BCI5P86H) (Active Moiety)
- LARIX DECIDUA FLOWERING TOP (UNII: 9UMZ642257)
- LARIX DECIDUA FLOWERING TOP (UNII: 9UMZ642257) (Active Moiety)
- MANGANESE (UNII: 42Z2K6ZL8P)
- MANGANESE (UNII: 42Z2K6ZL8P) (Active Moiety)
- MIMULUS GUTTATUS FLOWERING TOP (UNII: 192426I5JU)
- MIMULUS GUTTATUS FLOWERING TOP (UNII: 192426I5JU) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- RHUS AROMATICA ROOT BARK (UNII: Q3H36W0J42)
- RHUS AROMATICA ROOT BARK (UNII: Q3H36W0J42) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- ULEX EUROPAEUS FLOWER (UNII: 398DBS1PXN)
- ULEX EUROPAEUS FLOWER (UNII: 398DBS1PXN) (Active Moiety)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- BENZOIC ACID (UNII: 8SKN0B0MIM) (Active Moiety)
- COBALT (UNII: 3G0H8C9362)
- COBALT (UNII: 3G0H8C9362) (Active Moiety)
Which are Kidney Drainage 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 Kidney Drainage?
- Allergens - [CS]
- Allergens - [CS]
- Ammonium Ion Binding Activity - [MoA] (Mechanism of Action)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Nitrogen Binding Agent - [EPC] (Established Pharmacologic Class)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
- Vegetable Proteins - [CS]
* 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".