NDC 61589-6015 No7 Lift And Luminate Foundation Sunscreen Broad Spectrum Spf 15 Warm Ivory
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61589 - Bcm Cosmetique Sas
- 61589-6015 - No7 Lift And Luminate Foundation Sunscreen Broad Spectrum Spf 15 Warm Ivory
Product Packages
NDC Code 61589-6015-1
Package Description: 1 BOTTLE in 1 CARTON / 30 g in 1 BOTTLE
Product Details
What is NDC 61589-6015?
What are the uses for No7 Lift And Luminate Foundation Sunscreen Broad Spectrum Spf 15 Warm Ivory?
Which are No7 Lift And Luminate Foundation Sunscreen Broad Spectrum Spf 15 Warm Ivory 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 Warm Ivory 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)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK)
- 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 ACETATE (UNII: 9E8X80D2L0)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- ACTINIDIA CHINENSIS WHOLE (UNII: 8HTD3WU8LH)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (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)
- CARBOMER 934 (UNII: Z135WT9208)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- TOCOPHEROL (UNII: R0ZB2556P8)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- 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".