NDC 63083-6044 Plastics/bpa Detox 6044
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63083-6044?
What are the uses for Plastics/bpa Detox 6044?
Which are Plastics/bpa Detox 6044 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARCTIUM LAPPA ROOT OIL (UNII: 55DGS3F5YG)
- ARCTIUM LAPPA ROOT OIL (UNII: 55DGS3F5YG) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (Active Moiety)
- BOS TAURUS BRAIN (UNII: A1YEE2DB8Z)
- BOS TAURUS BRAIN (UNII: A1YEE2DB8Z) (Active Moiety)
- BEEF KIDNEY (UNII: 5HOC10FSIC)
- BEEF KIDNEY (UNII: 5HOC10FSIC) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV)
- BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV) (Active Moiety)
- BISPHENOL A (UNII: MLT3645I99)
- BISPHENOL A (UNII: MLT3645I99) (Active Moiety)
- METHYL METHACRYLATE (UNII: 196OC77688)
- METHYL METHACRYLATE (UNII: 196OC77688) (Active Moiety)
- CARBONATE ION (UNII: 7UJQ5OPE7D)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- SODIUM POLYSTYRENE SULFONATE (UNII: 1699G8679Z)
- POLYSTYRENE SULFONIC ACID (UNII: 70KO0R01RY) (Active Moiety)
- TRIS(2-ETHYLHEXYL)PHOSPHATE (UNII: BQC0BKB72S)
- TRIS(2-ETHYLHEXYL)PHOSPHATE (UNII: BQC0BKB72S) (Active Moiety)
Which are Plastics/bpa Detox 6044 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* 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".