NDC 40046-0050 Studio Fix Fluid Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 40046-0050?
Which are Studio Fix Fluid Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Studio Fix Fluid Spf 15 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TRIMETHYLSILANE (UNII: 9L70DJH2K0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- SEAWEED (UNII: 477TV3P5UX)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- LAURETH-7 (UNII: Z95S6G8201)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- SORBIC ACID (UNII: X045WJ989B)
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- CHROMIC OXIDE (UNII: X5Z09SU859)
* 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".