NDC 51531-4189 Foundation Primer Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 51531-4189?
What are the uses for Foundation Primer Spf 15?
Which are Foundation Primer Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Foundation Primer 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:
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- CERESIN (UNII: Q1LS2UJO3A)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- FRUIT (UNII: C2AIY4ERZC)
- FERULA ASSA-FOETIDA ROOT (UNII: 3U9288P88T)
- SUNFLOWER SEED (UNII: R9N3379M4Z)
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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".