NDC 51523-050 Thefaceshop Color Control Cushion Apricot Beige Oil-free Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51523 - Thefaceshop Co., Ltd.
- 51523-050 - Thefaceshop Color Control Cushion Apricot Beige
Product Packages
NDC Code 51523-050-01
Package Description: 2 CONTAINER in 1 BOX / 15 g in 1 CONTAINER
Product Details
What is NDC 51523-050?
What are the uses for Thefaceshop Color Control Cushion Apricot Beige Oil-free Spf 50?
Which are Thefaceshop Color Control Cushion Apricot Beige Oil-free Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
Which are Thefaceshop Color Control Cushion Apricot Beige Oil-free Spf 50 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:
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PALMITOYL PROLINE (UNII: I49727TDYF)
- TANGERINE PEEL (UNII: JU3D414057)
- ADENOSINE (UNII: K72T3FS567)
- MAGNESIUM PALMITOYL GLUTAMATE (UNII: DH37YM1F48)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MICA (UNII: V8A1AW0880)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- SODIUM PALMITOYL SARCOSINATE (UNII: 7297LY09YF)
- PALMITIC ACID (UNII: 2V16EO95H1)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- ALBIZIA JULIBRISSIN BARK (UNII: 0J9G6W44DV)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- WATER (UNII: 059QF0KO0R)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- METHYL METHACRYLATE (UNII: 196OC77688)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
- ZINC STEARATE (UNII: H92E6QA4FV)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- DISTEARYLDIMONIUM (UNII: 251IW5I21C)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- NIACINAMIDE (UNII: 25X51I8RD4)
- TROMETHAMINE (UNII: 023C2WHX2V)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SORBITAN SESQUIISOSTEARATE (UNII: VU97D01BF9)
* 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".