NDC 51514-0354 Solaire Peau Parfaite 100% Mineral Fluid Flawless Skin
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What is NDC 51514-0354?
What are the uses for Solaire Peau Parfaite 100% Mineral Fluid Flawless Skin?
Which are Solaire Peau Parfaite 100% Mineral Fluid Flawless Skin UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Solaire Peau Parfaite 100% Mineral Fluid Flawless Skin 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:
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CALCIUM GLUCONATE (UNII: SQE6VB453K)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- BENTONITE (UNII: A3N5ZCN45C)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- SEA SALT (UNII: 87GE52P74G)
- POLYGLYCERYL-2 MONOISOSTEARATE (UNII: 7B8OE71MQC)
- ARGAN OIL (UNII: 4V59G5UW9X)
- LINGONBERRY (UNII: 0UNK9RZQ7X)
- SQUALENE (UNII: 7QWM220FJH)
- LEVOMENOL (UNII: 24WE03BX2T)
- XANTHAN GUM (UNII: TTV12P4NEE)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- CHLORELLA VULGARIS (UNII: RYQ4R60M02)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- KAPPAPHYCUS ALVAREZII (UNII: T479H08K2O)
- KAKADU PLUM (UNII: 0ZQ1D2FDLI)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- OLIVE OIL DECYL ESTERS (UNII: 3AQ222F18X)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- LACTIC ACID, DL- (UNII: 3B8D35Y7S4)
- GLYCERIN (UNII: PDC6A3C0OX)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
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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".