NDC 50181-0043 Radiation
Chelidonium Majus,Fucus Vesiculosus,Hypericum Perforatum,Sulphur,Cesium Chloride,Glandula - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50181 - The Wellness Center For Research And Education, Inc.
- 50181-0043 - Radiation
Product Packages
NDC Code 50181-0043-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 50181-0043?
What are the uses for Radiation?
What are Radiation Active Ingredients?
- ALCOHOL, X-RAY EXPOSED (1000 RAD) 8 [hp_X]/mL
- CADMIUM IODIDE 8 [hp_X]/mL
- CADMIUM SULFATE 8 [hp_X]/mL
- CESIUM CHLORIDE 6 [hp_X]/mL
- CHELIDONIUM MAJUS 3 [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).
- FUCUS VESICULOSUS 3 [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.
- HYPERICUM PERFORATUM 6 [hp_X]/mL
- LACTOSE 30 [hp_C]/mL - A disaccharide of GLUCOSE and GALACTOSE in human and cow milk. It is used in pharmacy for tablets, in medicine as a nutrient, and in industry.
- PLUTONIUM 30 [hp_C]/mL - A naturally radioactive element of the actinide metals series. It has the atomic symbol Pu, and atomic number 94. Plutonium is used as a nuclear fuel, to produce radioisotopes for research, in radionuclide batteries for pacemakers, and as the agent of fission in nuclear weapons.
- RADIUM BROMIDE 15 [hp_X]/mL
- STRONTIUM CARBONATE 8 [hp_X]/mL
- SULFUR 6 [hp_X]/mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
- SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
- SUS SCROFA THYROID 8 [hp_X]/mL
- URANYL NITRATE HEXAHYDRATE 8 [hp_C]/mL
Which are Radiation UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- CESIUM CHLORIDE (UNII: GNR9HML8BA)
- CESIUM CATION (UNII: LCC4BG14DM) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)
- STRONTIUM CARBONATE (UNII: 41YPU4MMCA)
- STRONTIUM CATION (UNII: 37077S2C93) (Active Moiety)
- CADMIUM IODIDE (UNII: 2F2UPU4KCW)
- CADMIUM CATION (UNII: T494FZ4G8G) (Active Moiety)
- CADMIUM SULFATE (UNII: 947UNF3Z6O)
- ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P)
- ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P) (Active Moiety)
- RADIUM BROMIDE (UNII: R74O7T8569)
- RADIUM CATION (UNII: 05456MVL7T) (Active Moiety)
- URANYL NITRATE HEXAHYDRATE (UNII: 3V057702FY)
- URANIUM CATION (6+) (UNII: 5PI36AS4G7) (Active Moiety)
- LACTOSE (UNII: J2B2A4N98G)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) (Active Moiety)
- PLUTONIUM (UNII: 53023GN24M)
- PLUTONIUM (UNII: 53023GN24M) (Active Moiety)
Which are Radiation 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)
* 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.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[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".