NDC 0642-0076 Vitafol-ob Plus Dha Prenatal Supplement Plus Dha
Vitamin A,Ascorbic Acid,Vitamin D,.alpha.-tocopherol,Thiamine - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0642 - Exeltis Usa, Inc
- 0642-0076 - Vitafol-ob Plus Dha
Product Characteristics
YELLOW (C48330 - AMBER)
15 MM
Product Packages
NDC Code 0642-0076-03
Package Description: 1 KIT in 1 CARTON * 30 TABLET, COATED in 1 BOX * 30 CAPSULE in 1 BOX
NDC Code 0642-0076-30
Package Description: 1 KIT in 1 CARTON * 30 TABLET, COATED in 1 BOX * 30 CAPSULE in 1 BOX
Price per Unit: $2.08600 per EA
Product Details
What is NDC 0642-0076?
What are the uses for Vitafol-ob Plus Dha Prenatal Supplement Plus Dha?
Which are Vitafol-ob Plus Dha Prenatal Supplement Plus Dha UNII Codes?
The UNII codes for the active ingredients in this product are:
- VITAMIN A (UNII: 81G40H8B0T)
- VITAMIN A (UNII: 81G40H8B0T) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- VITAMIN D (UNII: 9VU1KI44GP)
- CHOLECALCIFEROL (UNII: 1C6V77QF41) (Active Moiety)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) (Active Moiety)
- THIAMINE MONONITRATE (UNII: 8K0I04919X)
- THIAMINE ION (UNII: 4ABT0J945J) (Active Moiety)
- RIBOFLAVIN (UNII: TLM2976OFR)
- RIBOFLAVIN (UNII: TLM2976OFR) (Active Moiety)
- NIACIN (UNII: 2679MF687A)
- NIACIN (UNII: 2679MF687A) (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 (UNII: SY7Q814VUP)
- CALCIUM (UNII: SY7Q814VUP) (Active Moiety)
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
- MAGNESIUM (UNII: I38ZP9992A)
- MAGNESIUM (UNII: I38ZP9992A) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC (UNII: J41CSQ7QDS) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- DOCONEXENT (UNII: ZAD9OKH9JC)
- DOCONEXENT (UNII: ZAD9OKH9JC) (Active Moiety)
Which are Vitafol-ob Plus Dha Prenatal Supplement Plus Dha 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- GELATIN (UNII: 2G86QN327L)
- CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T)
- SUCROSE (UNII: C151H8M554)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM ASCORBATE (UNII: S033EH8359)
- TOCOPHEROL (UNII: R0ZB2556P8)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ACACIA (UNII: 5C5403N26O)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SORBIC ACID (UNII: X045WJ989B)
- TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- TRIACETIN (UNII: XHX3C3X673)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Vitafol-ob Plus Dha Prenatal Supplement Plus Dha?
- RxCUI: 1100198 - docosahexaenoic acid 250 MG Oral Capsule
- RxCUI: 1100198 - DHA 250 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".