NDC 42546-518 Pr Natal 430 Ec
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42546 - Prugen, Inc Pharmaceuticals
- 42546-518 - Pr Natal 430 Ec
Product Characteristics
BROWN (C48332)
NONE
Product Packages
NDC Code 42546-518-30
Package Description: 1 KIT in 1 KIT * 30 TABLET in 1 BOTTLE * 30 CAPSULE, GELATIN COATED in 1 BOTTLE
Product Details
What is NDC 42546-518?
What are the uses for Pr Natal 430 Ec?
Which are Pr Natal 430 Ec UNII Codes?
The UNII codes for the active ingredients in this product are:
- 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)
- IRON PROTEIN SUCCINYLATE (UNII: VBJ9L90P4L)
- IRON PROTEIN SUCCINYLATE (UNII: VBJ9L90P4L) (Active Moiety)
- FERROUS BISGLYCINATE HYDROCHLORIDE (UNII: IW3QLZ8MRC)
- IRON (UNII: E1UOL152H7) (Active Moiety)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- CUPRIC OXIDE (UNII: V1XJQ704R4)
- CUPRIC OXIDE (UNII: V1XJQ704R4) (Active Moiety)
- OMEGA-3 FATTY ACIDS (UNII: 71M78END5S)
- OMEGA-3 FATTY ACIDS (UNII: 71M78END5S) (Active Moiety)
* 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".