NDC 13537-079 Lbel Effet Parfait Mineral Natural Skin Effect Mousse Foundation Spf 16 Claire 3- Beige
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 13537-079?
What are the uses for Lbel Effet Parfait Mineral Natural Skin Effect Mousse Foundation Spf 16 Claire 3- Beige?
Which are Lbel Effet Parfait Mineral Natural Skin Effect Mousse Foundation Spf 16 Claire 3- Beige 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 Mousse Foundation Spf 16 Claire 3- Beige 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)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- 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)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- LAUROYL LYSINE (UNII: 113171Q70B)
- PETROLATUM (UNII: 4T6H12BN9U)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- SEDUM ROSEUM ROOT (UNII: 3S5ITS5ULN)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CARNOSINE (UNII: 8HO6PVN24W)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- CANDELILLA WAX (UNII: WL0328HX19)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
- ALANYL GLUTAMINE (UNII: U5JDO2770Z)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
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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".