NDC 0642-3010 Reaphirm Plant Source Dha
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0642 - Everett Laboratories, Inc.
- 0642-3010 - Reaphirm Plant Source Dha
Product Characteristics
Product Packages
NDC Code 0642-3010-30
Package Description: 5 BLISTER PACK in 1 BOX / 6 CAPSULE, GELATIN COATED in 1 BLISTER PACK
Price per Unit: $2.98498 per EA
Product Details
What is NDC 0642-3010?
What are the uses for Reaphirm Plant Source Dha?
Which are Reaphirm Plant Source Dha UNII Codes?
The UNII codes for the active ingredients in this product are:
- VITAMIN A (UNII: 81G40H8B0T)
- BETA CAROTENE (UNII: 01YAE03M7J) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- THIAMINE MONONITRATE (UNII: 8K0I04919X)
- THIAMINE (UNII: X66NSO3N35) (Active Moiety)
- RIBOFLAVIN (UNII: TLM2976OFR)
- RIBOFLAVIN (UNII: TLM2976OFR) (Active Moiety)
- NIACIN (UNII: 2679MF687A)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- CYANOCOBALAMIN (UNII: P6YC3EG204) (Active Moiety)
- FOLIC ACID (UNII: 935E97BOY8)
- FOLIC ACID (UNII: 935E97BOY8) (Active Moiety)
- IODINE (UNII: 9679TC07X4)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- MAGNESIUM (UNII: I38ZP9992A)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- CUPRIC OXIDE (UNII: V1XJQ704R4) (Active Moiety)
- VITAMIN D (UNII: 9VU1KI44GP)
- CHOLECALCIFEROL (UNII: 1C6V77QF41) (Active Moiety)
- OMEGA-3 FATTY ACIDS (UNII: 71M78END5S)
- DOCONEXENT (UNII: ZAD9OKH9JC) (Active Moiety)
- VITAMIN E (UNII: H4N855PNZ1)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) (Active Moiety)
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
Which are Reaphirm Plant Source 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 (UNII: 2G86QN327L)
- SORBITOL (UNII: 506T60A25R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SOYBEAN OIL (UNII: 241ATL177A)
- WATER (UNII: 059QF0KO0R)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SODIUM THIOSULFATE (UNII: HX1032V43M)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- CARAMEL (UNII: T9D99G2B1R)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- CORN OIL (UNII: 8470G57WFM)
* 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".