NDC 0178-0891 Citranatal Assure
Ascorbic Acid,Calcium Citrate,Iron,Vitamin D,Dl- Alpha- Tocopherol - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0178 - Mission Pharmacal Company
- 0178-0891 - Citranatal Assure
Product Characteristics
ORANGE (C48331 - CARAMEL COLOR)
CAPSULE (C48336)
23 MM
Product Packages
NDC Code 0178-0891-30
Package Description: 30 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK
Price per Unit: $2.02408 per EA
Product Details
What is NDC 0178-0891?
What are the uses for Citranatal Assure?
Which are Citranatal Assure UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- CHOLECALCIFEROL (UNII: 1C6V77QF41) (Active Moiety)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) (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)
- IODINE (UNII: 9679TC07X4)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC (UNII: J41CSQ7QDS) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- DOCUSATE (UNII: M7P27195AG) (Active Moiety)
- THIAMINE (UNII: X66NSO3N35)
- THIAMINE ION (UNII: 4ABT0J945J) (Active Moiety)
- CALCIUM CITRATE (UNII: MLM29U2X85)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- DOCONEXENT (UNII: ZAD9OKH9JC)
- DOCONEXENT (UNII: ZAD9OKH9JC) (Active Moiety)
- ICOSAPENT (UNII: AAN7QOV9EA)
- ICOSAPENT (UNII: AAN7QOV9EA) (Active Moiety)
Which are Citranatal Assure 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:
- POVIDONE K30 (UNII: U725QWY32X)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SHELLAC (UNII: 46N107B71O)
- VANILLIN (UNII: CHI530446X)
- GELATIN (UNII: 2G86QN327L)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- GLYCERIN (UNII: PDC6A3C0OX)
- LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
- ROSEMARY (UNII: IJ67X351P9)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
What is the NDC to RxNorm Crosswalk for Citranatal Assure?
- RxCUI: 1535150 - docosaenoic acid 300 MG / eicosapentaenoic acid 0.75 MG Oral Capsule
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".