NDC 43742-0490 Liver Drainage
Chelidonium Majus,Carduus Marianus,Schisandra Chinensis,Taraxacum Officinale,Berberis - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-0490 - Liver Drainage
Product Packages
NDC Code 43742-0490-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-0490?
What are the uses for Liver Drainage?
What are Liver Drainage Active Ingredients?
- BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
- CHELIDONIUM MAJUS 1 [hp_X]/mL - A plant species of the family PAPAVERACEAE. The common name greater celandine is similar to lesser celandine (Ficaria verna), and celandine poppy (Stylophorum diphyllum). It has been used in folk medicine and its latex contains biologically active compounds including BENZOPHENANTHRIDINES alkaloids (e.g., Chelerythrine).
- CHROMIUM GLUCONATE 6 [hp_X]/mL
- CICHORIUM INTYBUS FLOWER 8 [hp_X]/mL
- COBALTOUS GLUCONATE 6 [hp_X]/mL
- COPPER GLUCONATE 6 [hp_X]/mL - Derivatives of gluconic acid (the structural formula HOCH2(CHOH)4COOH), including its salts and esters.
- LACTIC ACID, L- 6 [hp_X]/mL
- MAGNESIUM GLUCONATE 6 [hp_X]/mL
- MILK THISTLE 2 [hp_X]/mL
- NEOPICRORHIZA SCROPHULARIIFLORA ROOT 3 [hp_X]/mL
- PHENOL 8 [hp_X]/mL - An antiseptic and disinfectant aromatic alcohol.
- PORK LIVER 8 [hp_X]/mL
- PTELEA TRIFOLIATA BARK 6 [hp_X]/mL
- RADISH 3 [hp_X]/mL
- SCHISANDRA CHINENSIS FRUIT 2 [hp_X]/mL
- SODIUM SULFATE 6 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 8 [hp_X]/mL
- SULFUR IODIDE 6 [hp_X]/mL
- SUS SCROFA GALLBLADDER 8 [hp_X]/mL
- SUS SCROFA PANCREAS 8 [hp_X]/mL
- TARAXACUM OFFICINALE 2 [hp_X]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
- VANADIUM 8 [hp_X]/mL - A metallic element with the atomic symbol V, atomic number 23, and atomic weight 50.94. It is used in the manufacture of vanadium steel. Prolonged exposure can lead to chronic intoxication caused by absorption usually via the lungs.
- VERBENA OFFICINALIS FLOWERING TOP 8 [hp_X]/mL
- VISCUM ALBUM FRUITING TOP 3 [hp_X]/mL
Which are Liver Drainage UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- MILK THISTLE (UNII: U946SH95EE)
- MILK THISTLE (UNII: U946SH95EE) (Active Moiety)
- SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)
- SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- NEOPICRORHIZA SCROPHULARIIFLORA ROOT (UNII: K5P3MVJ81Q)
- NEOPICRORHIZA SCROPHULARIIFLORA ROOT (UNII: K5P3MVJ81Q) (Active Moiety)
- RADISH (UNII: EM5RP35463)
- RADISH (UNII: EM5RP35463) (Active Moiety)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (Active Moiety)
- CHROMIUM GLUCONATE (UNII: V236ZVR3RL)
- CHROMIC CATION (UNII: X1N4508KF1) (Active Moiety)
- COBALTOUS GLUCONATE (UNII: 26SK597UWV)
- COBALTOUS CATION (UNII: AI1MR454XG) (Active Moiety)
- COPPER GLUCONATE (UNII: RV823G6G67)
- CUPRIC CATION (UNII: 8CBV67279L) (Active Moiety)
- MAGNESIUM GLUCONATE (UNII: T42NAD2KHC)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- PTELEA TRIFOLIATA BARK (UNII: 5KQR6FTT0D)
- PTELEA TRIFOLIATA BARK (UNII: 5KQR6FTT0D) (Active Moiety)
- LACTIC ACID, L- (UNII: F9S9FFU82N)
- LACTIC ACID, L- (UNII: F9S9FFU82N) (Active Moiety)
- SULFUR IODIDE (UNII: L6L8KA2AA0)
- SULFUR IODIDE (UNII: L6L8KA2AA0) (Active Moiety)
- PHENOL (UNII: 339NCG44TV)
- PHENOL (UNII: 339NCG44TV) (Active Moiety)
- CICHORIUM INTYBUS FLOWER (UNII: HW54500A89)
- CICHORIUM INTYBUS FLOWER (UNII: HW54500A89) (Active Moiety)
- SUS SCROFA GALLBLADDER (UNII: B6A98VOI9I)
- SUS SCROFA GALLBLADDER (UNII: B6A98VOI9I) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- SUS SCROFA PANCREAS (UNII: 9Y3J3362RY)
- SUS SCROFA PANCREAS (UNII: 9Y3J3362RY) (Active Moiety)
- VANADIUM (UNII: 00J9J9XKDE)
- VANADIUM (UNII: 00J9J9XKDE) (Active Moiety)
- VERBENA OFFICINALIS FLOWERING TOP (UNII: 311PNK9CDZ)
- VERBENA OFFICINALIS FLOWERING TOP (UNII: 311PNK9CDZ) (Active Moiety)
Which are Liver 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 Liver Drainage?
- Allergens - [CS]
- Allergens - [CS]
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
- Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
- 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".