NDC 68807-307 Sun Protection Emulsion Face Broad Spectrum Spf 30 La Prairie Group
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68807 - Temmentec Ag
- 68807-307 - Sun Protection Emulsion Face Broad Spectrum Spf 30
Product Packages
NDC Code 68807-307-02
Package Description: 1 TUBE in 1 CARTON / 125 mL in 1 TUBE (68807-307-01)
Product Details
What is NDC 68807-307?
What are the uses for Sun Protection Emulsion Face Broad Spectrum Spf 30 La Prairie Group?
Which are Sun Protection Emulsion Face Broad Spectrum Spf 30 La Prairie Group UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Sun Protection Emulsion Face Broad Spectrum Spf 30 La Prairie Group 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)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- HEXYLDECANOL (UNII: 151Z7P1317)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- STEARETH-21 (UNII: 53J3F32P58)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GLYCERIN (UNII: PDC6A3C0OX)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CORALLINA OFFICINALIS (UNII: 4004498D06)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- STEARETH-2 (UNII: V56DFE46J5)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BENZYLIDENE DIMETHOXYDIMETHYLINDANONE (UNII: 75HIF3C97L)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SQUALANE (UNII: GW89575KF9)
- CARBOMER 934 (UNII: Z135WT9208)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- DULSE (UNII: 7832HOY4ZQ)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- PELVETIA CANALICULATA (UNII: 8U1M44KESN)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ALCOHOL (UNII: 3K9958V90M)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
* 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".