NDC 43742-1479 Gi Drainage
Cinnamomum,Gentiana Lutea,Syzygium Jambolanum,Argentum Nitricum,Colchicum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43742-1479?
What are the uses for Gi Drainage?
What are Gi Drainage Active Ingredients?
- ACTIVATED CHARCOAL 8 [hp_X]/mL
- ARCTIUM LAPPA ROOT 6 [hp_X]/mL
- BOS TAURUS COLOSTRUM 6 [hp_X]/mL
- CINNAMON 3 [hp_X]/mL
- COLCHICUM AUTUMNALE BULB 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.
- FAGUS SYLVATICA FLOWERING TOP 12 [hp_X]/mL
- GENTIANA LUTEA ROOT 3 [hp_X]/mL
- GOLD 8 [hp_X]/mL - A yellow metallic element with the atomic symbol Au, atomic number 79, and atomic weight 197. It is used in jewelry, goldplating of other metals, as currency, and in dental restoration. Many of its clinical applications, such as ANTIRHEUMATIC AGENTS, are in the form of its salts.
- LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/mL
- MAGNESIUM GLUCONATE 6 [hp_X]/mL
- MALUS PUMILA FLOWER 8 [hp_X]/mL
- MANGANESE GLUCONATE 6 [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)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X]/mL
- PORK INTESTINE 8 [hp_X]/mL
- POTASSIUM GLUCONATE 6 [hp_X]/mL
- PRUNUS CERASIFERA FLOWER 8 [hp_X]/mL
- RUMEX CRISPUS ROOT 6 [hp_X]/mL
- SCROPHULARIA NODOSA 6 [hp_X]/mL
- SILVER NITRATE 6 [hp_X]/mL - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.
- SUS SCROFA STOMACH 6 [hp_X]/mL
- SYZYGIUM CUMINI SEED 3 [hp_X]/mL
- WATER 8 [hp_X]/mL - A clear, odorless, tasteless liquid that is essential for most animal and plant life and is an excellent solvent for many substances. The chemical formula is hydrogen oxide (H2O). (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Which are Gi Drainage UNII Codes?
The UNII codes for the active ingredients in this product are:
- CINNAMON (UNII: 5S29HWU6QB)
- CINNAMON (UNII: 5S29HWU6QB) (Active Moiety)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS) (Active Moiety)
- SYZYGIUM CUMINI SEED (UNII: 820LSF646I)
- SYZYGIUM CUMINI SEED (UNII: 820LSF646I) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
- BOS TAURUS COLOSTRUM (UNII: S256WJ3OFQ)
- BOS TAURUS COLOSTRUM (UNII: S256WJ3OFQ) (Active Moiety)
- COPPER GLUCONATE (UNII: RV823G6G67)
- CUPRIC CATION (UNII: 8CBV67279L) (Active Moiety)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- MAGNESIUM GLUCONATE (UNII: T42NAD2KHC)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- MANGANESE GLUCONATE (UNII: 9YY2F980SV)
- MANGANESE CATION (2+) (UNII: H6EP7W5457) (Active Moiety)
- POTASSIUM GLUCONATE (UNII: 12H3K5QKN9)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (Active Moiety)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (Active Moiety)
- SUS SCROFA STOMACH (UNII: T0920P9Z9A)
- SUS SCROFA STOMACH (UNII: T0920P9Z9A) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- PORK INTESTINE (UNII: 40GMI0R60L)
- PORK INTESTINE (UNII: 40GMI0R60L) (Active Moiety)
- MALUS PUMILA FLOWER (UNII: EF626V855K)
- MALUS DOMESTICA FLOWER (UNII: EF626V855K) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS)
- PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS) (Active Moiety)
- WATER (UNII: 059QF0KO0R)
- WATER (UNII: 059QF0KO0R) (Active Moiety)
- FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U)
- FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U) (Active Moiety)
Which are Gi 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:
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Gi Drainage?
- Allergens - [CS]
- Allergens - [CS]
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [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)
- Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
- Potassium Compounds - [CS]
- Potassium Salt - [EPC] (Established Pharmacologic Class)
- Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
- 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".