NDC 59088-162 Diatrol
Vitamins And Mineral Capsule Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 59088-162?
What are the uses for Diatrol?
What are Diatrol Active Ingredients?
- .ALPHA.-TOCOPHEROL ACETATE, DL- 13.5 mg/1
- ARGININE HYDROCHLORIDE 60 ug/1 - An essential amino acid that is physiologically active in the L-form.
- ASCORBIC ACID 50 mg/1 - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
- BIOTIN 30 ug/1 - A water-soluble, enzyme co-factor present in minute amounts in every living cell. It occurs mainly bound to proteins or polypeptides and is abundant in liver, kidney, pancreas, yeast, and milk.
- CHOLECALCIFEROL 18.75 ug/1 - Derivative of 7-dehydroxycholesterol formed by ULTRAVIOLET RAYS breaking of the C9-C10 bond. It differs from ERGOCALCIFEROL in having a single bond between C22 and C23 and lacking a methyl group at C24.
- CHROMIUM NICOTINATE 200 ug/1
- GYMNEMA SYLVESTRE LEAF 100 mg/1
- LEVOMEFOLATE CALCIUM 1000 ug/1
- METHYLCOBALAMIN 8 ug/1
- NIACIN 24 mg/1 - A water-soluble vitamin of the B complex occurring in various animal and plant tissues. It is required by the body for the formation of coenzymes NAD and NADP. It has PELLAGRA-curative, vasodilating, and antilipemic properties.
- PANTOTHENIC ACID 8 mg/1 - A butyryl-beta-alanine that can also be viewed as pantoic acid complexed with BETA ALANINE. It is incorporated into COENZYME A and protects cells against peroxidative damage by increasing the level of GLUTATHIONE.
- PHYTONADIONE 90 ug/1
- PYRIDOXINE HYDROCHLORIDE 8 mg/1 - The 4-methanol form of VITAMIN B 6 which is converted to PYRIDOXAL PHOSPHATE which is a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. Although pyridoxine and Vitamin B 6 are still frequently used as synonyms, especially by medical researchers, this practice is erroneous and sometimes misleading (EE Snell; Ann NY Acad Sci, vol 585 pg 1, 1990).
- RIBOFLAVIN 4 mg/1 - Nutritional factor found in milk, eggs, malted barley, liver, kidney, heart, and leafy vegetables. The richest natural source is yeast. It occurs in the free form only in the retina of the eye, in whey, and in urine; its principal forms in tissues and cells are as FLAVIN MONONUCLEOTIDE and FLAVIN-ADENINE DINUCLEOTIDE.
- THIAMINE MONONITRATE 4 mg/1 - 3-((4-Amino-2-methyl-5-pyrimidinyl)methyl)-5-(2- hydroxyethyl)-4-methylthiazolium chloride.
- VANADYL SULFATE 15 mg/1
- VITAMIN A 900 ug/1 - Retinol and derivatives of retinol that play an essential role in metabolic functioning of the retina, the growth of and differentiation of epithelial tissue, the growth of bone, reproduction, and the immune response. Dietary vitamin A is derived from a variety of CAROTENOIDS found in plants. It is enriched in the liver, egg yolks, and the fat component of dairy products.
Which are Diatrol UNII Codes?
The UNII codes for the active ingredients in this product are:
- BIOTIN (UNII: 6SO6U10H04)
- BIOTIN (UNII: 6SO6U10H04) (Active Moiety)
- CHROMIUM NICOTINATE (UNII: A150AY412V)
- CHROMIC CATION (UNII: X1N4508KF1) (Active Moiety)
- GYMNEMA SYLVESTRE LEAF (UNII: 2ZK6ZS8392)
- GYMNEMA SYLVESTRE LEAF (UNII: 2ZK6ZS8392) (Active Moiety)
- ARGININE HYDROCHLORIDE (UNII: F7LTH1E20Y)
- ARGININE (UNII: 94ZLA3W45F) (Active Moiety)
- VANADYL SULFATE (UNII: 6DU9Y533FA)
- VANADIUM (UNII: 00J9J9XKDE) (Active Moiety)
- PHYTONADIONE (UNII: A034SE7857)
- PHYTONADIONE (UNII: A034SE7857) (Active Moiety)
- VITAMIN A (UNII: 81G40H8B0T)
- VITAMIN A (UNII: 81G40H8B0T) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- CHOLECALCIFEROL (UNII: 1C6V77QF41) (Active Moiety)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) (Active Moiety)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- THIAMINE MONONITRATE (UNII: 8K0I04919X)
- THIAMINE ION (UNII: 4ABT0J945J) (Active Moiety)
- RIBOFLAVIN (UNII: TLM2976OFR)
- RIBOFLAVIN (UNII: TLM2976OFR) (Active Moiety)
- NIACIN (UNII: 2679MF687A)
- NIACIN (UNII: 2679MF687A) (Active Moiety)
- LEVOMEFOLATE CALCIUM (UNII: A9R10K3F2F)
- LEVOMEFOLIC ACID (UNII: 8S95DH25XC) (Active Moiety)
- METHYLCOBALAMIN (UNII: BR1SN1JS2W)
- METHYLCOBALAMIN (UNII: BR1SN1JS2W) (Active Moiety)
- PANTOTHENIC ACID (UNII: 19F5HK2737)
- PANTOTHENIC ACID (UNII: 19F5HK2737) (Active Moiety)
Which are Diatrol 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
Which are the Pharmacologic Classes for Diatrol?
- Analogs/Derivatives - [Chemical/Ingredient]
- Ascorbic Acid - [CS]
- Folate Analog - [EPC] (Established Pharmacologic Class)
- Folic Acid - [CS]
- Increased Prothrombin Activity - [PE] (Physiologic Effect)
- Nicotinic Acid - [EPC] (Established Pharmacologic Class)
- Nicotinic Acids - [CS]
- Reversed Anticoagulation Activity - [PE] (Physiologic Effect)
- Vitamin A - [CS]
- Vitamin A - [EPC] (Established Pharmacologic Class)
- Vitamin B 6 - [Chemical/Ingredient]
- Vitamin B6 Analog - [EPC] (Established Pharmacologic Class)
- Vitamin C - [EPC] (Established Pharmacologic Class)
- Vitamin D - [CS]
- Vitamin D - [EPC] (Established Pharmacologic Class)
- Vitamin K - [CS]
- Vitamin K - [EPC] (Established Pharmacologic Class)
- Warfarin Reversal Agent - [EPC] (Established Pharmacologic Class)
* 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".