NDC 69417-110 Silken Pore Perfecting Sunscreen Broad Spectrum Spf 35
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69417 - Tatcha Inc.
- 69417-110 - Silken Pore Perfecting Sunscreen Broad Spectrum Spf 35
Product Packages
NDC Code 69417-110-03
Package Description: 1 TUBE in 1 CARTON / 10 g in 1 TUBE
NDC Code 69417-110-20
Package Description: 1 TUBE in 1 CARTON / 60 g in 1 TUBE
Product Details
What is NDC 69417-110?
What are the uses for Silken Pore Perfecting Sunscreen Broad Spectrum Spf 35?
Which are Silken Pore Perfecting Sunscreen Broad Spectrum Spf 35 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Silken Pore Perfecting Sunscreen Broad Spectrum Spf 35 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)
- ISODODECANE (UNII: A8289P68Y2)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- PROPANEDIOL (UNII: 5965N8W85T)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- ROSA MULTIFLORA FRUIT (UNII: EZ5DSL4T27)
- ERIOBOTRYA JAPONICA LEAF (UNII: Z02066SV11)
- STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
- GLYCYRRHIZA ECHINATA ROOT (UNII: V6E722P1VB)
- CAMELLIA JAPONICA LEAF (UNII: 4E3VE6KTLY)
- PISTACIA LENTISCUS RESIN (UNII: 7446H202QW)
- SILK SERICIN (UNII: 0N1VMU8G9W)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- INOSITOL (UNII: 4L6452S749)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- SORBITAN TRISTEARATE (UNII: 6LUM696811)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- BEHENETH-20 (UNII: BJ4GP2IFLN)
- SODIUM ACRYLATE (UNII: 7C98FKB43H)
- POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
- DIMETHICONOL (40 CST) (UNII: 343C7U75XW)
- BROWN IRON OXIDE (UNII: 1N032N7MFO)
- MICA (UNII: V8A1AW0880)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ALCOHOL (UNII: 3K9958V90M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
* 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".