NDC 64141-111 Skin Foundation Mineral Makeup Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 64141-111?
Which are Skin Foundation Mineral 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)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Skin Foundation Mineral 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:
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- SOYBEAN (UNII: L7HT8F1ZOD)
- PANTHENOL (UNII: WV9CM0O67Z)
- CERAMIDE 2 (UNII: C04977SRJ5)
- CERAMIDE 3 (UNII: 4370DF050B)
- GLYCERIN (UNII: PDC6A3C0OX)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TRIMETHYLSILANE (UNII: 9L70DJH2K0)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- LAURETH-12 (UNII: OAH19558U1)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- MICA (UNII: V8A1AW0880)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
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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".