NDC 40046-0057 Studio Foundation Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 40046-0057?
Which are Studio Foundation 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 Foundation 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:
- DI-PPG-3 MYRISTYL ETHER ADIPATE (UNII: T32481VTXW)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- PROPYLENE GLYCOL MONOLAURATE (UNII: 668Z5835Z3)
- PROPYLENE GLYCOL STEARATE (UNII: MZM1I680W0)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".