NDC 42192-323 Pnv-dha
Ascorbic Acid,Cholecalciferol,.alpha.-tocopherol Acetate,Dl-,Pyridoxine,Folic - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42192 - Acella Pharmaceuticals, Llc
- 42192-323 - Pnv-dha
Product Characteristics
Product Packages
NDC Code 42192-323-30
Package Description: 30 CAPSULE, GELATIN COATED in 1 BOTTLE
Price per Unit: $1.07660 per EA
Product Details
What is NDC 42192-323?
What are the uses for Pnv-dha?
What are Pnv-dha Active Ingredients?
- .ALPHA.-TOCOPHEROL ACETATE, DL- 30 [iU]/1
- ASCORBIC ACID 28 mg/1 - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
- CALCIUM 160 mg/1 - A basic element found in nearly all tissues. It is a member of the alkaline earth family of metals with the atomic symbol Ca, atomic number 20, and atomic weight 40. Calcium is the most abundant mineral in the body and combines with phosphorus to form calcium phosphate in the bones and teeth. It is essential for the normal functioning of nerves and muscles and plays a role in blood coagulation (as factor IV) and in many enzymatic processes.
- CHOLECALCIFEROL 400 [iU]/1 - Derivative of 7-dehydroxycholesterol formed by ULTRAVIOLET RAYS breaking of the C9-C10 bond. It differs from ERGOCALCIFEROL in having a single bond between C22 and C23 and lacking a methyl group at C24.
- DOCONEXENT 300 mg/1
- FERROUS FUMARATE 27 mg/1
- FOLIC ACID 1.25 mg/1 - A member of the vitamin B family that stimulates the hematopoietic system. It is present in the liver and kidney and is found in mushrooms, spinach, yeast, green leaves, and grasses (POACEAE). Folic acid is used in the treatment and prevention of folate deficiencies and megaloblastic anemia.
- PYRIDOXINE 25 mg/1 - The 4-methanol form of VITAMIN B 6 which is converted to PYRIDOXAL PHOSPHATE which is a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. Although pyridoxine and Vitamin B 6 are still frequently used as synonyms, especially by medical researchers, this practice is erroneous and sometimes misleading (EE Snell; Ann NY Acad Sci, vol 585 pg 1, 1990).
Which are Pnv-dha UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- CALCIUM (UNII: SY7Q814VUP)
- CALCIUM (UNII: SY7Q814VUP) (Active Moiety)
- FERROUS FUMARATE (UNII: R5L488RY0Q)
- FERROUS CATION (UNII: GW89581OWR) (Active Moiety)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- CHOLECALCIFEROL (UNII: 1C6V77QF41) (Active Moiety)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) (Active Moiety)
- PYRIDOXINE (UNII: KV2JZ1BI6Z)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- FOLIC ACID (UNII: 935E97BOY8)
- FOLIC ACID (UNII: 935E97BOY8) (Active Moiety)
- DOCONEXENT (UNII: ZAD9OKH9JC)
- DOCONEXENT (UNII: ZAD9OKH9JC) (Active Moiety)
Which are Pnv-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:
- GELATIN TYPE B BOVINE (230 BLOOM) (UNII: WIL1404U79)
- GLYCERIN (UNII: PDC6A3C0OX)
- SOYBEAN OIL (UNII: 241ATL177A)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- WATER (UNII: 059QF0KO0R)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ORANGE (UNII: 5EVU04N5QU)
- ETHYL VANILLIN (UNII: YC9ST449YJ)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
Which are the Pharmacologic Classes for Pnv-dha?
- Analogs/Derivatives - [Chemical/Ingredient]
- Ascorbic Acid - [CS]
- Calcium - [CS]
- Calcium - [EPC] (Established Pharmacologic Class)
- Vitamin B 6 - [Chemical/Ingredient]
- Vitamin B6 Analog - [EPC] (Established Pharmacologic Class)
- Vitamin C - [EPC] (Established Pharmacologic Class)
- Vitamin D - [CS]
- Vitamin D - [EPC] (Established Pharmacologic Class)
* 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.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[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".