NDC 68807-323 Ultra Protection Stick Broad Spectrum Spf 40 La Prairie Switzerland
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68807 - Temmentec Ag
- 68807-323 - Ultra Protection Stick Broad Spectrum Spf 40
Product Packages
NDC Code 68807-323-11
Package Description: 78.4 kg in 1 DRUM
Product Details
What is NDC 68807-323?
What are the uses for Ultra Protection Stick Broad Spectrum Spf 40 La Prairie Switzerland?
Which are Ultra Protection Stick Broad Spectrum Spf 40 La Prairie Switzerland 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 Ultra Protection Stick Broad Spectrum Spf 40 La Prairie Switzerland 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:
- POLYETHYLENE GLYCOL 350 (UNII: ZBR3T82M2V)
- PETROLATUM (UNII: 4T6H12BN9U)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- JOJOBA BUTTER (UNII: XIA46H803R)
- WATER (UNII: 059QF0KO0R)
- SHEA BUTTER (UNII: K49155WL9Y)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- WHITE WAX (UNII: 7G1J5DA97F)
- PELVETIA CANALICULATA (UNII: 8U1M44KESN)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- DULSE (UNII: 7832HOY4ZQ)
- BEHENYL OLIVATE (UNII: NGS1GGK4GW)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- PORPHYRA UMBILICALIS (UNII: 14AN0J70WO)
- AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
- BENZYLIDENE DIMETHOXYDIMETHYLINDANONE (UNII: 75HIF3C97L)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ALCOHOL (UNII: 3K9958V90M)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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[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".