NDC 10096-0229 Ultra Color Rich Moisture Seduction
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10096 - Avon Products, Inc.
- 10096-0229 - Ultra Color Rich
Product Packages
NDC Code 10096-0229-1
Package Description: 3 g in 1 CASE
Product Details
What is NDC 10096-0229?
What are the uses for Ultra Color Rich Moisture Seduction?
Which are Ultra Color Rich Moisture Seduction UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Ultra Color Rich Moisture Seduction 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:
- SQUALANE (UNII: GW89575KF9)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- LANOLIN (UNII: 7EV65EAW6H)
- PETROLATUM (UNII: 4T6H12BN9U)
- SUCROSE ACETATE ISOBUTYRATE (UNII: H5KI1C3YTV)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- RETINOL (UNII: G2SH0XKK91)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- GLYCERIN (UNII: PDC6A3C0OX)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- ALLANTOIN (UNII: 344S277G0Z)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- HYALURONIC ACID (UNII: S270N0TRQY)
- WATER (UNII: 059QF0KO0R)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- LAUROYL LYSINE (UNII: 113171Q70B)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- UREA (UNII: 8W8T17847W)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- BETA CAROTENE (UNII: 01YAE03M7J)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- MICA (UNII: V8A1AW0880)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- BARIUM SULFATE (UNII: 25BB7EKE2E)
* 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".