NDC 68807-308 Sun Protection Body Sunscreen Broad Spectrum Spf 30 La Prairie
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68807 - Temmentec Ag
- 68807-308 - Sun Protection Body Sunscreen Broad Spectrum Spf 30
Product Packages
NDC Code 68807-308-02
Package Description: 1 TUBE in 1 CARTON / 180 mL in 1 TUBE (68807-308-01)
Product Details
What is NDC 68807-308?
What are the uses for Sun Protection Body Sunscreen Broad Spectrum Spf 30 La Prairie?
Which are Sun Protection Body Sunscreen Broad Spectrum Spf 30 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)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Sun Protection Body Sunscreen Broad Spectrum Spf 30 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)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- STEARETH-21 (UNII: 53J3F32P58)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALLANTOIN (UNII: 344S277G0Z)
- PORPHYRA UMBILICALIS (UNII: 14AN0J70WO)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BENZYLIDENE DIMETHOXYDIMETHYLINDANONE (UNII: 75HIF3C97L)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- PELVETIA CANALICULATA (UNII: 8U1M44KESN)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DULSE (UNII: 7832HOY4ZQ)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- STEARETH-2 (UNII: V56DFE46J5)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALCOHOL (UNII: 3K9958V90M)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- LAURETH-7 (UNII: Z95S6G8201)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- 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".