NDC 71407-002 Gesgep One Drop Perfection True
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 71407-002?
What are the uses for Gesgep One Drop Perfection True?
Which are Gesgep One Drop Perfection True UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Gesgep One Drop Perfection True 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- ISODODECANE (UNII: A8289P68Y2)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- NIACINAMIDE (UNII: 25X51I8RD4)
- LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- PANTHENOL (UNII: WV9CM0O67Z)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ADENOSINE (UNII: K72T3FS567)
- CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839)
- GLYCERIN (UNII: PDC6A3C0OX)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- PISTACIA LENTISCUS RESIN (UNII: 7446H202QW)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
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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".