NDC 68026-131 Skin Caviar Foundation Sunscreen Spf 15 - Golden Beige
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 68026-131?
What are the uses for Skin Caviar Foundation Sunscreen Spf 15 - Golden Beige?
Which are Skin Caviar Foundation Sunscreen Spf 15 - Golden Beige UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Skin Caviar Foundation Sunscreen Spf 15 - Golden Beige 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:
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- XANTHAN GUM (UNII: TTV12P4NEE)
- LYSINE (UNII: K3Z4F929H6)
- ARGININE (UNII: 94ZLA3W45F)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
- GLUCURONIC ACID (UNII: 8A5D83Q4RW)
- PROLINE (UNII: 9DLQ4CIU6V)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- METHIONINE (UNII: AE28F7PNPL)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- LAURYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EX0F4CZ66H)
- DIISOPROPYL DILINOLEATE (UNII: 5323S7S2LR)
- CITRONELLAL (UNII: QB99VZZ7GZ)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PSEUDEVERNIA FURFURACEA (UNII: 49ZMN09Q0K)
- BENZYL BENZOATE (UNII: N863NB338G)
- GERANIOL (UNII: L837108USY)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- LACTOBACILLUS REUTERI (UNII: 9913I24QEE)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
- GLYCINE (UNII: TE7660XO1C)
- CAVIAR, UNSPECIFIED (UNII: 020K6HLU0O)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- LACTOBACILLUS RHAMNOSUS (UNII: 9601IVB87J)
- TOCOPHEROL (UNII: R0ZB2556P8)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
- PETROLATUM (UNII: 4T6H12BN9U)
- SARGASSUM FILIPENDULA (UNII: 55P66J5H7N)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- SOYBEAN OIL (UNII: 241ATL177A)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- ETHYLPARABEN (UNII: 14255EXE39)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- PANTHENOL (UNII: WV9CM0O67Z)
- .ALPHA.-TOCOPHEROL LINOLEATE, D- (UNII: G0N132Q0ED)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- CERAMIDE 3 (UNII: 4370DF050B)
- WATER (UNII: 059QF0KO0R)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ETHYLHEXYL HYDROXYSTEARATE (UNII: B7I80BVV5E)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
- C18-36 ACID TRIGLYCERIDE (UNII: ZRA72DR3R7)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
* 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".