NDC 68807-315 White Caviar Illuminating Hand Sunscreen Broad Spectrum Spf 15 La Prairie
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68807 - Temmentec Ag
- 68807-315 - White Caviar Illuminating Hand Sunscreen Broad Spectrum Spf 15
Product Packages
NDC Code 68807-315-11
Package Description: 78.4 kg in 1 DRUM
Product Details
What is NDC 68807-315?
What are the uses for White Caviar Illuminating Hand Sunscreen Broad Spectrum Spf 15 La Prairie?
Which are White Caviar Illuminating Hand Sunscreen Broad Spectrum Spf 15 La Prairie UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (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 White Caviar Illuminating Hand Sunscreen Broad Spectrum Spf 15 La Prairie 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SHEA BUTTER (UNII: K49155WL9Y)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
- CAVIAR, UNSPECIFIED (UNII: 020K6HLU0O)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- PHORMIDIUM PERSICINUM (UNII: ZA983U4810)
- ABELMOSCHUS MOSCHATUS SEED (UNII: UN2QZ55I88)
- RESVERATROL (UNII: Q369O8926L)
- LYSINE HYDROCHLORIDE (UNII: JNJ23Q2COM)
- THREONINE (UNII: 2ZD004190S)
- NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
- TRYPTOPHAN (UNII: 8DUH1N11BX)
- GARDEN CRESS SPROUT (UNII: PWQ18YNR62)
- HISTIDINE (UNII: 4QD397987E)
- SERINE (UNII: 452VLY9402)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- FOLIC ACID (UNII: 935E97BOY8)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- LEONTOPODIUM ALPINUM FLOWERING TOP (UNII: QQC1AK06RK)
- CARNOSINE (UNII: 8HO6PVN24W)
- SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)
- GLYCINE (UNII: TE7660XO1C)
- ARGININE (UNII: 94ZLA3W45F)
- HYDROXYETHYL BEHENAMIDOPROPYL DIMONIUM CHLORIDE (UNII: 9CO8OUL4TH)
- LICORICE (UNII: 61ZBX54883)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
- PANTHENOL (UNII: WV9CM0O67Z)
- SODIUM OLEATE (UNII: 399SL044HN)
- XANTHAN GUM (UNII: TTV12P4NEE)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BUTYL STEARATE (UNII: 6Y0AI5605C)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- GERANIOL (UNII: L837108USY)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- BENZYL BENZOATE (UNII: N863NB338G)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- EUGENOL (UNII: 3T8H1794QW)
- FARNESOL (UNII: EB41QIU6JL)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
* 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".