NDC 76049-620 Stila Illuminate And Shine
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76049-620?
What are the uses for Stila Illuminate And Shine?
Which are Stila Illuminate And Shine UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Stila Illuminate And Shine 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)
- DIETHYLHEXYL CARBONATE (UNII: YCD50O0Z6L)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- DIISOSTEAROYL POLYGLYCERYL-3 DIMER DILINOLEATE (UNII: G3232Z5S2O)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALMOND OIL (UNII: 66YXD4DKO9)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SORBIC ACID (UNII: X045WJ989B)
- ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- MICA (UNII: V8A1AW0880)
- 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".