NDC 82668-110 Alix Avien Vegan Matte Foundation
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82668 - Alix Avien Kozmetik Sanayi Ticaret Anonim Sirketi
- 82668-110 - Alix Avien
Product Packages
NDC Code 82668-110-01
Package Description: 1 TUBE in 1 CARTON / 30 mL in 1 TUBE
Product Details
What is NDC 82668-110?
What are the uses for Alix Avien Vegan Matte Foundation?
Which are Alix Avien Vegan Matte Foundation UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Alix Avien Vegan Matte 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:
- WATER (UNII: 059QF0KO0R)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- OLEYL ALCOHOL (UNII: 172F2WN8DV)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- HYDROGENATED OLIVE OIL (UNII: 53839415GI)
- NYLON-12 (UNII: 446U8J075B)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- QUATERNIUM-90 SEPIOLITE (UNII: J9ULC97SE5)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- QUATERNIUM-90 MONTMORILLONITE (UNII: 7BL4KVZ54U)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PROPANEDIOL (UNII: 5965N8W85T)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TROLAMINE (UNII: 9O3K93S3TK)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ARTEMISIA CAPILLARIS FLOWER (UNII: KG4724BPZG)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- 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".