NDC 10477-2627 Tinted Spf 45
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 10477-2627?
What are the uses for Tinted Spf 45?
Which are Tinted Spf 45 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)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Tinted Spf 45 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)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- SORBITOL (UNII: 506T60A25R)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BETULA PUBESCENS BARK (UNII: 3R504894L9)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- WHITE WAX (UNII: 7G1J5DA97F)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SQUALANE (UNII: GW89575KF9)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
- UBIDECARENONE (UNII: EJ27X76M46)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- SORBIC ACID (UNII: X045WJ989B)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
* 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".