NDC 50967-410 Nestabs One
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50967 - Womens Choice Pharmaceuticals, Llc
- 50967-410 - Nestabs One
Product Characteristics
Product Packages
NDC Code 50967-410-30
Package Description: 30 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 50967-410?
What are the uses for Nestabs One?
Which are Nestabs One UNII Codes?
The UNII codes for the active ingredients in this product are:
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- FOLIC ACID (UNII: 935E97BOY8)
- FOLIC ACID (UNII: 935E97BOY8) (Active Moiety)
- ANTAZOLINE (UNII: DHA8014SS1)
- ANTAZOLINE (UNII: DHA8014SS1) (Active Moiety)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TOCOPHEROL (UNII: R0ZB2556P8) (Active Moiety)
- CALCIUM ASCORBATE (UNII: 183E4W213W)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- CYANOCOBALAMIN (UNII: P6YC3EG204) (Active Moiety)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- CHOLECALCIFEROL (UNII: 1C6V77QF41) (Active Moiety)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
Which are Nestabs One 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:
- WATER (UNII: 059QF0KO0R)
- GELATIN TYPE B BOVINE (160 BLOOM) (UNII: 1T8387508X)
- GLYCERIN (UNII: PDC6A3C0OX)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- WHITE WAX (UNII: 7G1J5DA97F)
* 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".