NDC 50090-0435 Multivitamin With Fluoride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 50090-0435?
What are the uses for Multivitamin With Fluoride?
Which are Multivitamin With Fluoride UNII Codes?
The UNII codes for the active ingredients in this product are:
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- CYANOCOBALAMIN (UNII: P6YC3EG204) (Active Moiety)
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- FOLIC ACID (UNII: 935E97BOY8)
- FOLIC ACID (UNII: 935E97BOY8) (Active Moiety)
- NIACIN (UNII: 2679MF687A)
- NIACIN (UNII: 2679MF687A) (Active Moiety)
- PYRIDOXINE (UNII: KV2JZ1BI6Z)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- RIBOFLAVIN (UNII: TLM2976OFR)
- RIBOFLAVIN (UNII: TLM2976OFR) (Active Moiety)
- THIAMINE (UNII: X66NSO3N35)
- THIAMINE ION (UNII: 4ABT0J945J) (Active Moiety)
- VITAMIN A (UNII: 81G40H8B0T)
- VITAMIN A (UNII: 81G40H8B0T) (Active Moiety)
- VITAMIN D (UNII: 9VU1KI44GP)
- VITAMIN D (UNII: 9VU1KI44GP) (Active Moiety)
Which are Multivitamin With Fluoride 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:
- XYLITOL (UNII: VCQ006KQ1E)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- MANNITOL (UNII: 3OWL53L36A)
- TALC (UNII: 7SEV7J4R1U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
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[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".