NDC 20151-063 Luxury Revitalizing Serum
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 20151-063?
What are the uses for Luxury Revitalizing Serum?
Which are Luxury Revitalizing Serum UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Luxury Revitalizing Serum 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 ANISATE (UNII: F9WFJ28MV9)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- WATER (UNII: 059QF0KO0R)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- PERFLUNAFENE (UNII: 54A06VV62N)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- SODIUM LEVULINATE (UNII: VK44E1MQU8)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- ETHYLBISIMINOMETHYLGUAIACOL MANGANESE CHLORIDE (UNII: SM5YJ88LTU)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
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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".