NDC 43742-1330 Systemic Drainage
Alfalfa,Avena Sativa,Citrus Limonum,Glycyrrhiza Glabra,Uva-ursi,Taraxacum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1330 - Systemic Drainage
Product Packages
NDC Code 43742-1330-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1330?
What are the uses for Systemic Drainage?
What are Systemic Drainage Active Ingredients?
- ALFALFA 1 [hp_X]/mL
- ARCTOSTAPHYLOS UVA-URSI LEAF 1 [hp_X]/mL
- AVENA SATIVA FLOWERING TOP 1 [hp_X]/mL
- BERBERIS VULGARIS ROOT BARK 6 [hp_X]/mL
- CHELIDONIUM MAJUS 6 [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).
- GALIUM APARINE 3 [hp_X]/mL - A genus of herbaceous annual and perennial plants in the family RUBIACEAE.
- GLYCYRRHIZA GLABRA 1 [hp_X]/mL - A genus of leguminous herbs or shrubs whose roots yield GLYCYRRHETINIC ACID and its derivative, CARBENOXOLONE.
- LACTIC ACID, DL- 12 [hp_X]/mL
- LACTIC ACID, L- 8 [hp_X]/mL
- LEMON JUICE 1 [hp_X]/mL
- MAGNESIUM GLUCONATE 6 [hp_X]/mL
- PORK INTESTINE 6 [hp_X]/mL
- PORK KIDNEY 6 [hp_X]/mL
- PORK LIVER 6 [hp_X]/mL
- POTASSIUM GLUCONATE 6 [hp_X]/mL
- SCHISANDRA CHINENSIS FRUIT 3 [hp_X]/mL
- SOLIDAGO VIRGAUREA FLOWERING TOP 3 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 8 [hp_X]/mL
- SUS SCROFA LUNG 6 [hp_X]/mL
- SUS SCROFA LYMPH 6 [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.
- TOBACCO LEAF 4 [hp_X]/mL
- TYLOPHORA INDICA LEAF 3 [hp_X]/mL
- ZINC GLUCONATE 6 [hp_X]/mL
Which are Systemic Drainage UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALFALFA (UNII: DJO934BRBD)
- ALFALFA (UNII: DJO934BRBD) (Active Moiety)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- LEMON JUICE (UNII: AGN709ANTJ)
- LEMON JUICE (UNII: AGN709ANTJ) (Active Moiety)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (Active Moiety)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- GALIUM APARINE (UNII: Z4B6561488)
- GALIUM APARINE (UNII: Z4B6561488) (Active Moiety)
- SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)
- SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
- TYLOPHORA INDICA LEAF (UNII: WG10XM3N5R)
- TYLOPHORA INDICA LEAF (UNII: WG10XM3N5R) (Active Moiety)
- TOBACCO LEAF (UNII: 6YR2608RSU)
- TOBACCO LEAF (UNII: 6YR2608RSU) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- PORK INTESTINE (UNII: 40GMI0R60L)
- PORK INTESTINE (UNII: 40GMI0R60L) (Active Moiety)
- PORK KIDNEY (UNII: X7BCI5P86H)
- PORK KIDNEY (UNII: X7BCI5P86H) (Active Moiety)
- SUS SCROFA LUNG (UNII: 7GL3G1COB3)
- SUS SCROFA LUNG (UNII: 7GL3G1COB3) (Active Moiety)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L) (Active Moiety)
- MAGNESIUM GLUCONATE (UNII: T42NAD2KHC)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- POTASSIUM GLUCONATE (UNII: 12H3K5QKN9)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- LACTIC ACID, L- (UNII: F9S9FFU82N)
- LACTIC ACID, L- (UNII: F9S9FFU82N) (Active Moiety)
- LACTIC ACID, DL- (UNII: 3B8D35Y7S4)
- LACTIC ACID, DL- (UNII: 3B8D35Y7S4) (Active Moiety)
Which are Systemic 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 Systemic Drainage?
- Allergens - [CS]
- Allergens - [CS]
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
- Decreased Copper Ion Absorption - [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]
- Potassium Compounds - [CS]
- Potassium Salt - [EPC] (Established Pharmacologic Class)
- Seed Storage Proteins - [CS]
- Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
* 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".