NDC 14783-220 Lbel Clarite Clarifying Effect Foundation Spf 30 Claire 7/beige
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What is NDC 14783-220?
What are the uses for Lbel Clarite Clarifying Effect Foundation Spf 30 Claire 7/beige?
Which are Lbel Clarite Clarifying Effect Foundation Spf 30 Claire 7/beige UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Lbel Clarite Clarifying Effect Foundation Spf 30 Claire 7/beige 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:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MICA (UNII: V8A1AW0880)
- STARCH, CORN (UNII: O8232NY3SJ)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- KOJIC DIPALMITATE (UNII: 13N249RWTM)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- LICORICE (UNII: 61ZBX54883)
- DIMETHYLMETHOXY CHROMANYL PALMITATE (UNII: 5G222ZDK7U)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
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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".