NDC 69677-050 Vita-rx Diabetic Vitamin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69677 - Mas Management Group Inc.
- 69677-050 - Vita-rx Diabetic Vitamin
Product Characteristics
Product Packages
NDC Code 69677-050-60
Package Description: 60 CAPSULE, GELATIN COATED in 1 PACKAGE
Product Details
What is NDC 69677-050?
What are the uses for Vita-rx Diabetic Vitamin?
Which are Vita-rx Diabetic Vitamin UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- CHOLECALCIFEROL (UNII: 1C6V77QF41) (Active Moiety)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) (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)
- PYRIDOXAL PHOSPHATE ANHYDROUS (UNII: F06SGE49M6)
- PYRIDOXAL 5-PHOSPHATE (UNII: F06SGE49M6) (Active Moiety)
- FOLIC ACID (UNII: 935E97BOY8)
- FOLIC ACID (UNII: 935E97BOY8) (Active Moiety)
- METHYLCOBALAMIN (UNII: BR1SN1JS2W)
- METHYLCOBALAMIN (UNII: BR1SN1JS2W) (Active Moiety)
- BIOTIN (UNII: 6SO6U10H04)
- BIOTIN (UNII: 6SO6U10H04) (Active Moiety)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- PANTOTHENIC ACID (UNII: 19F5HK2737) (Active Moiety)
- CHROMIUM PICOLINATE (UNII: S71T8B8Z6P)
- CHROMIC CATION (UNII: X1N4508KF1) (Active Moiety)
- ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y) (Active Moiety)
- UBIDECARENONE (UNII: EJ27X76M46)
- UBIDECARENONE (UNII: EJ27X76M46) (Active Moiety)
Which are Vita-rx Diabetic Vitamin 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:
- SODIUM METAVANADATE TETRAHYDRATE (UNII: 2DO8B1WW6L)
- GELATIN (UNII: 2G86QN327L)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[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".