NDC 0178-0859 Citranatal Rx
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0178 - Mission Pharmacal Company
- 0178-0859 - Citranatal Rx
Product Characteristics
Product Packages
NDC Code 0178-0859-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 0178-0859?
What are the uses for Citranatal Rx?
Which are Citranatal Rx UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- CALCIUM CITRATE (UNII: MLM29U2X85)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
- VITAMIN D (UNII: 9VU1KI44GP)
- CHOLECALCIFEROL (UNII: 1C6V77QF41) (Active Moiety)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) (Active Moiety)
- THIAMINE (UNII: X66NSO3N35)
- 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)
- POTASSIUM IODIDE (UNII: 1C4QK22F9J)
- IODIDE ION (UNII: 09G4I6V86Q) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- CUPRIC OXIDE (UNII: V1XJQ704R4)
- CUPRIC CATION (UNII: 8CBV67279L) (Active Moiety)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- DOCUSATE (UNII: M7P27195AG) (Active Moiety)
Which are Citranatal Rx 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:
- POVIDONES (UNII: FZ989GH94E)
- FERROUS GLUCONATE (UNII: U1B11I423Z)
- ALPHA-TOCOPHERYLQUINONE (UNII: ZO763K43XR)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- ETHYL VANILLIN (UNII: YC9ST449YJ)
* 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".