NDC 75854-322 Primacare
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75854 - Avion Pharmaceuticals, Llc
- 75854-322 - Primacare
Product Characteristics
Product Packages
NDC Code 75854-322-30
Package Description: 30 PILL in 1 BOTTLE
Product Details
What is NDC 75854-322?
What are the uses for Primacare?
Which are Primacare UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM ASCORBATE (UNII: 183E4W213W)
- 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)
- RIBOFLAVIN (UNII: TLM2976OFR)
- RIBOFLAVIN (UNII: TLM2976OFR) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- PYRIDOXINE (UNII: KV2JZ1BI6Z)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- FOLIC ACID (UNII: 935E97BOY8)
- FOLIC ACID (UNII: 935E97BOY8) (Active Moiety)
- BIOTIN (UNII: 6SO6U10H04)
- BIOTIN (UNII: 6SO6U10H04) (Active Moiety)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- POTASSIUM IODIDE (UNII: 1C4QK22F9J)
- IODIDE ION (UNII: 09G4I6V86Q) (Active Moiety)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC (UNII: J41CSQ7QDS) (Active Moiety)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- LINOLEIC ACID (UNII: 9KJL21T0QJ) (Active Moiety)
- OMEGA-3 FATTY ACIDS (UNII: 71M78END5S)
- OMEGA-3 FATTY ACIDS (UNII: 71M78END5S) (Active Moiety)
Which are Primacare 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:
- FERROUS ASPARTO GLYCINATE (UNII: H7426RGB3L)
- GELATIN (UNII: 2G86QN327L)
- SORBITOL (UNII: 506T60A25R)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
* 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".