NDC 52686-279 Shiseido Perfect Refining Foundation D30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52686 - Shiseido America Inc.
- 52686-279 - Shiseido Perfect Refining Foundation
Product Packages
NDC Code 52686-279-60
Package Description: 1 TUBE in 1 CARTON / 33.9 g in 1 TUBE
Product Details
What is NDC 52686-279?
What are the uses for Shiseido Perfect Refining Foundation D30?
Which are Shiseido Perfect Refining Foundation D30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Shiseido Perfect Refining Foundation D30 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)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- NYLON-12 (UNII: 446U8J075B)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- DIETHYLHEXYL SUCCINATE (UNII: 69W9UMG3P8)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- ERYTHRITOL (UNII: RA96B954X6)
- XYLITOL (UNII: VCQ006KQ1E)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ALUMINUM DISTEARATE (UNII: 7P1HP1B9UI)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- PEG/PPG-36/41 DIMETHYL ETHER (UNII: GZ406N3R9F)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- MICA (UNII: V8A1AW0880)
- DIPENTAERYTHRITYL HEXAHYDROXYSTEARATE (UNII: 74J1X57U42)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- BARIUM SULFATE (UNII: 25BB7EKE2E)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- TETRADECENE (UNII: FW23481S7S)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
* 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".