NDC 68327-005 Briteprep Fx
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68327-005?
What are the uses for Briteprep Fx?
Which are Briteprep Fx UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Briteprep 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)
- WATER (UNII: 059QF0KO0R)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- GLYCERIN (UNII: PDC6A3C0OX)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- TEA LEAF (UNII: GH42T47V24)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3.7) (UNII: 8INO2K35FA)
- SQUALANE (UNII: GW89575KF9)
- MICA (UNII: V8A1AW0880)
- GLYCERYL 1,2-DIBEHENATE (UNII: 21E45121YS)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- LEVOMENOL (UNII: 24WE03BX2T)
- SHEA BUTTER (UNII: K49155WL9Y)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- OCTADECENEDIOIC ACID (UNII: 565ZMT5QRG)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
- ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- LINOLENIC ACID (UNII: 0RBV727H71)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- TEPRENONE (UNII: S8S8451A4O)
- BRINE SHRIMP (UNII: 3ID50N77DH)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%) (UNII: 8136Y38GY5)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SORBIC ACID (UNII: X045WJ989B)
- CITRUS AURANTIUM FLOWER OIL (UNII: D4BGE91OXH)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
* 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".