NDC 68807-317 Anti-aging Eye Broad Spectrum Spf 15 La Prairie Switzerland
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What is NDC 68807-317?
What are the uses for Anti-aging Eye Broad Spectrum Spf 15 La Prairie Switzerland?
Which are Anti-aging Eye Broad Spectrum Spf 15 La Prairie Switzerland UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Anti-aging Eye Broad Spectrum Spf 15 La Prairie Switzerland 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)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SHEA BUTTER (UNII: K49155WL9Y)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)
- GLYCERYL CAPRATE (UNII: 197M6VFC1W)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
- HESPERETIN LAURATE (UNII: HP864VLN2T)
- TOCOPHEROL (UNII: R0ZB2556P8)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- URSOLIC ACID (UNII: P3M2575F3F)
- CARNOSINE (UNII: 8HO6PVN24W)
- ECHIUM PLANTAGINEUM SEED OIL (UNII: PIB7XBU8XW)
- CARBOMER 934 (UNII: Z135WT9208)
- CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
- SERINE (UNII: 452VLY9402)
- MILK THISTLE (UNII: U946SH95EE)
- ACACIA (UNII: 5C5403N26O)
- ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
- HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
- LAUROYL LYSINE (UNII: 113171Q70B)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- GLYCERIN (UNII: PDC6A3C0OX)
- TREHALOSE (UNII: B8WCK70T7I)
- POLYQUATERNIUM-51 (2-METHACRYLOYLOXYETHYL PHOSPHORYLCHOLINE/N-BUTYL METHACRYLATE; 3:7) (UNII: EL9825H96J)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- PEG-6 ISOSTEARATE (UNII: 0E2639OTJY)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- UREA (UNII: 8W8T17847W)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ISOPROPYLBENZYL SALICYLATE (UNII: 0798EIC152)
- STEARETH-2 (UNII: V56DFE46J5)
- CETETH-20 (UNII: I835H2IHHX)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TRIACETIN (UNII: XHX3C3X673)
- MICA (UNII: V8A1AW0880)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- STEARETH-21 (UNII: 53J3F32P58)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- SUCROSE (UNII: C151H8M554)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALCOHOL (UNII: 3K9958V90M)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- GERANIOL (UNII: L837108USY)
- BENZYL BENZOATE (UNII: N863NB338G)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ETHYLPARABEN (UNII: 14255EXE39)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
* 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".