NDC 11559-727 Nutritious Vita Mineral Loose Powder Makeup Spf 15
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What is NDC 11559-727?
Which are Nutritious Vita Mineral Loose Powder Makeup 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)
Which are Nutritious Vita Mineral Loose Powder Makeup 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:
- HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
- TALC (UNII: 7SEV7J4R1U)
- POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- MAGNESIUM MYRISTATE (UNII: Z1917F0578)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CALCIUM SILICATE (UNII: S4255P4G5M)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- ZINC STEARATE (UNII: H92E6QA4FV)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- MICA (UNII: V8A1AW0880)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FERRIC FERROCYANIDE (UNII: TLE294X33A)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- CHROMIC OXIDE (UNII: X5Z09SU859)
- COCHINEAL (UNII: TZ8Z31B35M)
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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".