NDC 52686-340 Shiseido Urban Environment Tinted Uv Protector 2
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What is NDC 52686-340?
What are the uses for Shiseido Urban Environment Tinted Uv Protector 2?
Which are Shiseido Urban Environment Tinted Uv Protector 2 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Shiseido Urban Environment Tinted Uv Protector 2 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PENTAERYTHRITYL TETRAETHYLHEXANOATE (UNII: XJ7052W897)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- XYLITOL (UNII: VCQ006KQ1E)
- POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- PEG/PPG-14/7 DIMETHYL ETHER (UNII: 6DNW9T7YT2)
- THIOTAURINE (UNII: NQZ2D7AO62)
- SAXIFRAGA STOLONIFERA LEAF (UNII: O3TMV4903H)
- ARGININE HYDROCHLORIDE (UNII: F7LTH1E20Y)
- ONONIS SPINOSA ROOT (UNII: FD2FMC53M1)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- PPG-17 (UNII: OV0Q322E0U)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- ALUMINUM DISTEARATE (UNII: 7P1HP1B9UI)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- TALC (UNII: 7SEV7J4R1U)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALCOHOL (UNII: 3K9958V90M)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SYZYGIUM JAMBOS LEAF (UNII: 407Z4W5LFF)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
* 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".