NDC 72940-0001 2 Transform
Fucus Vesiculosus,Chelidonium Majus,Kali Phosphoricum,Lycopodium Clavatum,Natrum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72940 - 2 Transform
- 72940-0001 - 2 Transform
Product Packages
NDC Code 72940-0001-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 72940-0001?
What are the uses for 2 Transform?
What are 2 Transform Active Ingredients?
- ACTIVATED CHARCOAL 12 [hp_X]/mL
- BERBERIS AQUIFOLIUM ROOT BARK 8 [hp_X]/mL
- BERBERIS VULGARIS ROOT BARK 8 [hp_X]/mL
- BOS TAURUS HYPOTHALAMUS 16 [hp_X]/mL
- CHASTE TREE FRUIT 8 [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).
- DIBASIC POTASSIUM PHOSPHATE 6 [hp_X]/mL
- FUCUS VESICULOSUS 4 [hp_X]/mL - A genus of BROWN ALGAE in the family Fucaceae. It is found in temperate, marine intertidal areas along rocky coasts and is a source of ALGINATES. Some species of Fucus are referred to as KELP.
- GRAPHITE 12 [hp_X]/mL - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
- LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/mL
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 12 [hp_X]/mL
- ORNITHOGALUM UMBELLATUM 8 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 6 [hp_X]/mL
- QUERCUS ROBUR NUT 6 [hp_X]/mL
- QUERCUS ROBUR TWIG BARK 6 [hp_X]/mL
- SINAPIS ARVENSIS FLOWERING/FRUITING TOP 12 [hp_X]/mL
- SODIUM CHLORIDE 6 [hp_X]/mL - A ubiquitous sodium salt that is commonly used to season food.
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 12 [hp_X]/mL
- SOLIDAGO VIRGAUREA FLOWERING TOP 8 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/mL
- SUCROSE 8 [hp_X]/mL - A nonreducing disaccharide composed of GLUCOSE and FRUCTOSE linked via their anomeric carbons. It is obtained commercially from SUGARCANE, sugar beet (BETA VULGARIS), and other plants and used extensively as a food and a sweetener.
- SUS SCROFA PITUITARY GLAND 12 [hp_X]/mL
- SUS SCROFA PLACENTA 12 [hp_X]/mL
- UBIDECARENONE 12 [hp_X]/mL
Which are 2 Transform UNII Codes?
The UNII codes for the active ingredients in this product are:
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- QUERCUS ROBUR NUT (UNII: Q7MU1F4GLY)
- QUERCUS ROBUR NUT (UNII: Q7MU1F4GLY) (Active Moiety)
- QUERCUS ROBUR TWIG BARK (UNII: 2JFK226947)
- QUERCUS ROBUR TWIG BARK (UNII: 2JFK226947) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- ORNITHOGALUM UMBELLATUM (UNII: 9NS3M2Y78S)
- ORNITHOGALUM UMBELLATUM (UNII: 9NS3M2Y78S) (Active Moiety)
- CHASTE TREE FRUIT (UNII: 433OSF3U8A)
- CHASTE TREE (UNII: 433OSF3U8A) (Active Moiety)
- BERBERIS AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB)
- BERBERIS AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- SUCROSE (UNII: C151H8M554)
- SUCROSE (UNII: C151H8M554) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (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)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
- SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK)
- SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK) (Active Moiety)
- UBIDECARENONE (UNII: EJ27X76M46)
- UBIDECARENONE (UNII: EJ27X76M46) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT)
- SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT) (Active Moiety)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8) (Active Moiety)
- BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7)
- BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7) (Active Moiety)
Which are 2 Transform 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:
- COPTIS CHINENSIS ROOT (UNII: CXS4LJR7EL)
- ARGININE (UNII: 94ZLA3W45F)
- CYSTEINE (UNII: K848JZ4886)
- LEUCINE (UNII: GMW67QNF9C)
- PROLINE (UNII: 9DLQ4CIU6V)
- SERINE (UNII: 452VLY9402)
- THREONINE (UNII: 2ZD004190S)
- VALINE (UNII: HG18B9YRS7)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for 2 Transform?
- Allergens - [CS]
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- 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 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)
* 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".