NDC 82574-001 Bop Whiteningtoothpaste
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 82574-001?
What are the uses for Bop Whiteningtoothpaste?
Which are Bop Whiteningtoothpaste UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- GLYCYRRHIZIN (UNII: 6FO62043WK) (Active Moiety)
- XYLITOL (UNII: VCQ006KQ1E)
- XYLITOL (UNII: VCQ006KQ1E) (Active Moiety)
Which are Bop Whiteningtoothpaste 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:
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- POLYETHYLENE GLYCOL 1600 (UNII: 1212Z7S33A)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- 5-METHYL-1,3,5-TRIPHENYL-2-PYRAZOLINE (UNII: 96K6O83026)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PISTACIA LENTISCUS RESIN (UNII: 7446H202QW)
- MENTHONE 1,2-GLYCEROL KETAL, (+/-)- (UNII: 7QQ1EE6RCP)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- SORBITOL (UNII: 506T60A25R)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- WATER (UNII: 059QF0KO0R)
- SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
- MENTHOL (UNII: L7T10EIP3A)
- CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
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[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".