NDC 61589-6003 No7 Lift And Luminate Foundation Sunscreen Broad Spectrum Spf 15 Wheat
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 61589-6003?
Which are No7 Lift And Luminate Foundation Sunscreen Broad Spectrum Spf 15 Wheat UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are No7 Lift And Luminate Foundation Sunscreen Broad Spectrum Spf 15 Wheat 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- TALC (UNII: 7SEV7J4R1U)
- MICA (UNII: V8A1AW0880)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- ACTINIDIA CHINENSIS WHOLE (UNII: 8HTD3WU8LH)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- AVENA SATIVA WHOLE (UNII: 5P8D0Z74RG)
- ETHYLPARABEN (UNII: 14255EXE39)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALCOHOL (UNII: 3K9958V90M)
- LUPINUS ALBUS SEED (UNII: 24GB753W3B)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- TOCOPHEROL (UNII: R0ZB2556P8)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* Please review the disclaimer below.
[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".