NDC 71110-0017 Anew Vitale Day
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 71110-0017?
What are the uses for Anew Vitale Day?
Which are Anew Vitale Day UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Anew Vitale Day 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:
- PANTHENOL (UNII: WV9CM0O67Z)
- MESYLOXYBENZYL METHOXYETHYL CHLOROBENZAMIDE (UNII: 3HB4C300XB)
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TRISILOXANE (UNII: 9G1ZW13R0G)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- DILAURYL THIODIPROPIONATE (UNII: V51YH1B080)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- THIODIPROPIONIC ACID (UNII: 3BBK323ED8)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- GLYCERIN (UNII: PDC6A3C0OX)
- ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- CHOLETH-24 (UNII: 5UE7I54O43)
- CETETH-24 (UNII: 0EV3Z43Y2I)
- DIMETHICONE (UNII: 92RU3N3Y1O)
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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".