NDC 14783-770 Lbel Effet Parfait Mineral Natural Skin Effect Mouse Foundation
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 14783-770?
What are the uses for Lbel Effet Parfait Mineral Natural Skin Effect Mouse Foundation?
Which are Lbel Effet Parfait Mineral Natural Skin Effect Mouse Foundation UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Lbel Effet Parfait Mineral Natural Skin Effect Mouse Foundation 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- MICA (UNII: V8A1AW0880)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- LAUROYL LYSINE (UNII: 113171Q70B)
- PETROLATUM (UNII: 4T6H12BN9U)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CARNOSINE (UNII: 8HO6PVN24W)
- CANDELILLA WAX (UNII: WL0328HX19)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- ALANYL-GLUTAMINE (UNII: U5JDO2770Z)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".