NDC 50090-0617 Pnv Prenatal Plus Multivitamin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-0617 - Pnv Prenatal Plus Multivitamin
Product Characteristics
Product Packages
NDC Code 50090-0617-0
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC
NDC Code 50090-0617-1
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 50090-0617?
What are the uses for Pnv Prenatal Plus Multivitamin?
Which are Pnv Prenatal Plus Multivitamin UNII Codes?
The UNII codes for the active ingredients in this product are:
- VITAMIN A ACETATE (UNII: 3LE3D9D6OY)
- VITAMIN A (UNII: 81G40H8B0T) (Active Moiety)
- .BETA.-CAROTENE (UNII: 01YAE03M7J)
- .BETA.-CAROTENE (UNII: 01YAE03M7J) (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)
- THIAMINE MONONITRATE (UNII: 8K0I04919X)
- THIAMINE ION (UNII: 4ABT0J945J) (Active Moiety)
- RIBOFLAVIN (UNII: TLM2976OFR)
- RIBOFLAVIN (UNII: TLM2976OFR) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- FOLIC ACID (UNII: 935E97BOY8)
- FOLIC ACID (UNII: 935E97BOY8) (Active Moiety)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- CYANOCOBALAMIN (UNII: P6YC3EG204) (Active Moiety)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- FERROUS FUMARATE (UNII: R5L488RY0Q)
- FERROUS CATION (UNII: GW89581OWR) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- CUPRIC OXIDE (UNII: V1XJQ704R4)
- CUPRIC CATION (UNII: 8CBV67279L) (Active Moiety)
Which are Pnv Prenatal Plus Multivitamin 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- TALC (UNII: 7SEV7J4R1U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
* 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".