NDC 52686-271 Shiseido Urban Environment Uv Protection
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 52686-271?
What are the uses for Shiseido Urban Environment Uv Protection?
Which are Shiseido Urban Environment Uv Protection UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Shiseido Urban Environment Uv Protection 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)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- XYLITOL (UNII: VCQ006KQ1E)
- METHYL GLUCETH-10 (UNII: N0MWT4C7WH)
- THIOTAURINE (UNII: NQZ2D7AO62)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- ARGININE HYDROCHLORIDE (UNII: F7LTH1E20Y)
- ONONIS SPINOSA ROOT (UNII: FD2FMC53M1)
- ECTOINE (UNII: 7GXZ3858RY)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SYZYGIUM JAMBOS LEAF (UNII: 407Z4W5LFF)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
* 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".