NDC 43857-0567 Bio Electrolyte
Boron Citrate,Calcium Gluconate,Chromium Picolinate,Cobalt Gluconate,Copper - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43857-0567?
What are the uses for Bio Electrolyte?
What are Bio Electrolyte Active Ingredients?
- BORON CITRATE 6 [hp_X]/mL
- CALCIUM GLUCONATE 6 [hp_X]/mL - The calcium salt of gluconic acid. The compound has a variety of uses, including its use as a calcium replenisher in hypocalcemic states.
- CHROMIUM PICOLINATE 6 [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.
- DIBASIC POTASSIUM PHOSPHATE 8 [hp_X]/mL
- FERROUS SULFATE 8 [hp_X]/mL
- MAGNESIUM GLUCONATE 6 [hp_X]/mL
- MANGANESE GLUCONATE 6 [hp_X]/mL
- NICKEL ACETATE 6 [hp_X]/mL
- POTASSIUM GLUCONATE 6 [hp_X]/mL
- SELENIUM DIOXIDE 6 [hp_X]/mL - Inorganic compounds formed through the oxidation of selenium.
- SODIUM GLUCONATE 6 [hp_X]/mL
- TRIBASIC CALCIUM PHOSPHATE 9 [hp_X]/mL
- 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.
- ZINC GLUCONATE 6 [hp_X]/mL
Which are Bio Electrolyte UNII Codes?
The UNII codes for the active ingredients in this product are:
- BORON CITRATE (UNII: S043P4DV22)
- BORON (UNII: N9E3X5056Q) (Active Moiety)
- CALCIUM GLUCONATE (UNII: SQE6VB453K)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CHROMIUM PICOLINATE (UNII: S71T8B8Z6P)
- 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)
- MANGANESE GLUCONATE (UNII: 9YY2F980SV)
- MANGANESE CATION (2+) (UNII: H6EP7W5457) (Active Moiety)
- NICKEL ACETATE (UNII: 99QP4ELX96)
- NICKEL CATION (UNII: OIS2CXW7AM) (Active Moiety)
- POTASSIUM GLUCONATE (UNII: 12H3K5QKN9)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- SELENIUM DIOXIDE (UNII: 9N3UK29E57)
- SELENIUM DIOXIDE (UNII: 9N3UK29E57) (Active Moiety)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- GLUCONIC ACID (UNII: R4R8J0Q44B) (Active Moiety)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- FERROUS SULFATE (UNII: 39R4TAN1VT)
- FERROUS CATION (UNII: GW89581OWR) (Active Moiety)
- DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- VANADIUM (UNII: 00J9J9XKDE)
- VANADIUM (UNII: 00J9J9XKDE) (Active Moiety)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
Which are Bio Electrolyte 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:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- DEXTROSE MONOHYDRATE (UNII: LX22YL083G)
- ALCOHOL (UNII: 3K9958V90M)
- ARGININE (UNII: 94ZLA3W45F)
- LEVOCARNITINE (UNII: 0G389FZZ9M)
- LEUCINE (UNII: GMW67QNF9C)
- ORNITHINE HYDROCHLORIDE (UNII: HBK84K66XH)
- VALINE (UNII: HG18B9YRS7)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- WATER (UNII: 059QF0KO0R)
- WINE GRAPE JUICE (UNII: JHQ6158A7R)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
Which are the Pharmacologic Classes for Bio Electrolyte?
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cations, Divalent - [CS]
- Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
- Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
- Increased Coagulation Factor Activity - [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)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
- Potassium Compounds - [CS]
- Potassium Salt - [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.
[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".