NDC 59158-913 Prescriptives Site Unseen Brightening Concealer Broad Spectrum Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 59158-913?
What are the uses for Prescriptives Site Unseen Brightening Concealer Broad Spectrum Spf 15?
Which are Prescriptives Site Unseen Brightening Concealer Broad Spectrum 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)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Prescriptives Site Unseen Brightening Concealer Broad Spectrum 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- YEAST (UNII: 3NY3SM6B8U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- GLYCERIN (UNII: PDC6A3C0OX)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- VALYLTRYPTOPHAN (UNII: 3G64B4AFQN)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
- LAURETH-7 (UNII: Z95S6G8201)
- ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- HESPERIDIN METHYLCHALCONE (UNII: 4T2GVA922X)
- STEARETH-20 (UNII: L0Q8IK9E08)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MICA (UNII: V8A1AW0880)
- 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".