NDC 68327-003 Skin Tint Fx
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68327-003?
What are the uses for Skin Tint Fx?
Which are Skin Tint Fx UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Skin Tint Fx 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- SQUALANE (UNII: GW89575KF9)
- TRIDECYL TRIMELLITATE (UNII: FY36J270ES)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- MICA (UNII: V8A1AW0880)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
- LEVOMENOL (UNII: 24WE03BX2T)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DIMETHICONOL (41 MPA.S) (UNII: 343C7U75XW)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERIN (UNII: PDC6A3C0OX)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- LINOLENIC ACID (UNII: 0RBV727H71)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- PEG/PPG-20/15 DIMETHICONE (UNII: 06R6X77P9C)
- CERAMIDE 2 (UNII: C04977SRJ5)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- PEG-10 RAPESEED STEROL (UNII: 258O76T85M)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SORBIC ACID (UNII: X045WJ989B)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CHROMIC OXIDE (UNII: X5Z09SU859)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
* 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".