NDC 43596-0012 Lbel Effet Parfait Spots Reducing Effect Foundation Spf 18 - Medium 6
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 43596-0012?
What are the uses for Lbel Effet Parfait Spots Reducing Effect Foundation Spf 18 - Medium 6?
Which are Lbel Effet Parfait Spots Reducing Effect Foundation Spf 18 - Medium 6 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Lbel Effet Parfait Spots Reducing Effect Foundation Spf 18 - Medium 6 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:
- ISOSTEARYL NEOPENTANOATE (UNII: 411THY156Q)
- MICA (UNII: V8A1AW0880)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CERESIN (UNII: Q1LS2UJO3A)
- KAOLIN (UNII: 24H4NWX5CO)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- STARCH, CORN (UNII: O8232NY3SJ)
- KOJIC DIPALMITATE (UNII: 13N249RWTM)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SHEA BUTTER (UNII: K49155WL9Y)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- .BETA.-SITOSTEROL (UNII: S347WMO6M4)
- CANDELILLA WAX (UNII: WL0328HX19)
- TRIMETHYLSILOXYSILICATE (M/Q 0.66) (UNII: 5041RX63GN)
- PETROLATUM (UNII: 4T6H12BN9U)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- WHITE WAX (UNII: 7G1J5DA97F)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* 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".