NDC 51523-112 Face It Radiance Two Way Cake Nb21
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51523 - Thefaceshop Co., Ltd
- 51523-112 - Face It Radiance Two Way Cake Nb21
Product Packages
NDC Code 51523-112-02
Package Description: 1 CONTAINER in 1 BOX / 11 g in 1 CONTAINER (51523-112-01)
Product Details
What is NDC 51523-112?
Which are Face It Radiance Two Way Cake Nb21 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Face It Radiance Two Way Cake Nb21 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:
- MICA (UNII: V8A1AW0880)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ALUMINUM DIMYRISTATE (UNII: J2KA067N9O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- GLYCERIN (UNII: PDC6A3C0OX)
- LAUROYL LYSINE (UNII: 113171Q70B)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- BENZIMIDAZOLE (UNII: E24GX49LD8)
- MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
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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".