NDC 68807-310 Cellular Swiss Uv Protection Veil Sunscreen Broad Spectrum Spf 50 La Prairie
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68807-310?
What are the uses for Cellular Swiss Uv Protection Veil Sunscreen Broad Spectrum Spf 50 La Prairie?
Which are Cellular Swiss Uv Protection Veil Sunscreen Broad Spectrum Spf 50 La Prairie UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Cellular Swiss Uv Protection Veil Sunscreen Broad Spectrum Spf 50 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SQUALANE (UNII: GW89575KF9)
- NYLON-12 (UNII: 446U8J075B)
- GLYCOPROTEIN HORMONES ALPHA CHAIN (UNII: 8YJ68CQ409)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- GLYCERIN (UNII: PDC6A3C0OX)
- CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- LEONTOPODIUM NIVALE SUBSP. ALPINUM FLOWER (UNII: MWN6IZU3XM)
- ROSA MULTIFLORA FRUIT (UNII: EZ5DSL4T27)
- LICORICE (UNII: 61ZBX54883)
- SODIUM METHYL STEAROYL TAURATE (UNII: JFM219LJ55)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- XANTHAN GUM (UNII: TTV12P4NEE)
- HIBISCUS SABDARIFFA FLOWER (UNII: 45TGG6IU6M)
- MORUS ALBA BARK (UNII: 7O71A48NDP)
- CUCUMBER SEED (UNII: BT3S9L53JK)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- LACTOBACILLUS REUTERI (UNII: 9913I24QEE)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- ALCOHOL (UNII: 3K9958V90M)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- PSEUDEVERNIA FURFURACEA (UNII: 49ZMN09Q0K)
- BENZYL BENZOATE (UNII: N863NB338G)
- GERANIOL (UNII: L837108USY)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- EUGENOL (UNII: 3T8H1794QW)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
* 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".