NDC 40046-0042 Mineralize Satin Foundation Spf 15 Foundation
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 40046-0042?
Which are Mineralize Satin Foundation Spf 15 Foundation UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Mineralize Satin Foundation Spf 15 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SQUALANE (UNII: GW89575KF9)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- GLYCERIN (UNII: PDC6A3C0OX)
- KAOLIN (UNII: 24H4NWX5CO)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- BEET (UNII: N487KM8COK)
- YEAST (UNII: 3NY3SM6B8U)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- LYSINE (UNII: K3Z4F929H6)
- ALPHA-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
- PANTHENOL (UNII: WV9CM0O67Z)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- TROMETHAMINE (UNII: 023C2WHX2V)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- 2-OCTANOL (UNII: 66B0DD5E40)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* 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".