NDC 68807-316 Anti-aging Day Broad Spectrum Spf 30 La Prairie Group Ag
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 68807-316?
What are the uses for Anti-aging Day Broad Spectrum Spf 30 La Prairie Group Ag?
Which are Anti-aging Day Broad Spectrum Spf 30 La Prairie Group Ag 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)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Anti-aging Day Broad Spectrum Spf 30 La Prairie Group Ag 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- STEARETH-21 (UNII: 53J3F32P58)
- DOCOSANOL (UNII: 9G1OE216XY)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SALICORNIA EUROPAEA (UNII: 6ADL50JAKW)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- RESVERATROL (UNII: Q369O8926L)
- TREHALOSE (UNII: B8WCK70T7I)
- UREA (UNII: 8W8T17847W)
- LARIX SIBIRICA WOOD (UNII: KSC3PGF73L)
- CARNOSINE (UNII: 8HO6PVN24W)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- MYROTHAMNUS FLABELLIFOLIA LEAF (UNII: 6Y9E0R40J5)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CHLORELLA VULGARIS (UNII: RYQ4R60M02)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PANTHENOL (UNII: WV9CM0O67Z)
- POLYQUATERNIUM-51 (2-METHACRYLOYLOXYETHYL PHOSPHORYLCHOLINE/N-BUTYL METHACRYLATE; 3:7) (UNII: EL9825H96J)
- SOYBEAN OIL (UNII: 241ATL177A)
- PEG-100 STEARATE (UNII: YD01N1999R)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- ALLANTOIN (UNII: 344S277G0Z)
- HYDROXYETHYL BEHENAMIDOPROPYL DIMONIUM CHLORIDE (UNII: 9CO8OUL4TH)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM OLEATE (UNII: 399SL044HN)
- LAURETH-7 (UNII: Z95S6G8201)
- CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- STEARETH-2 (UNII: V56DFE46J5)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- CARBOMER 934 (UNII: Z135WT9208)
- SYNTHETIC WAX (1800 MW) (UNII: 248P1AUJ90)
- ALCOHOL (UNII: 3K9958V90M)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- GERANIOL (UNII: L837108USY)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- BENZYL BENZOATE (UNII: N863NB338G)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- PSEUDEVERNIA FURFURACEA (UNII: 49ZMN09Q0K)
- EUGENOL (UNII: 3T8H1794QW)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SORBIC ACID (UNII: X045WJ989B)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
* 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".