NDC 49527-735 Clinique Spf 15 With Solar Smart Advanced Protection
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 49527-735?
Which are Clinique Spf 15 With Solar Smart Advanced Protection UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Clinique Spf 15 With Solar Smart Advanced 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- TRIACONTANYL PVP (WP-660) (UNII: N0SS3Q238D)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ROSEMARY (UNII: IJ67X351P9)
- PERILLA FRUTESCENS LEAF (UNII: T4L5881Y68)
- CAFFEINE (UNII: 3G6A5W338E)
- SUCROSE (UNII: C151H8M554)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROMETHAMINE (UNII: 023C2WHX2V)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- MASOPROCOL (UNII: 7BO8G1BYQU)
- FERULIC ACID (UNII: AVM951ZWST)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- MICA (UNII: V8A1AW0880)
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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".