NDC 14783-083 Lbel Couleur Luxe Supreme Xp
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What is NDC 14783-083?
What are the uses for Lbel Couleur Luxe Supreme Xp?
Which are Lbel Couleur Luxe Supreme Xp UNII Codes?
The UNII codes for the active ingredients in this product are:
- 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 Lbel Couleur Luxe Supreme Xp 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:
- CASTOR OIL (UNII: D5340Y2I9G)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DECYL OLEATE (UNII: ZGR06DO97T)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CANDELILLA WAX (UNII: WL0328HX19)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ARACHIDYL PROPIONATE (UNII: QV5DAH3MSB)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ETHYL LINOLEATE (UNII: MJ2YTT4J8M)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- D&C RED NO. 6 (UNII: 481744AI4O)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- TALC (UNII: 7SEV7J4R1U)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- OLEYL ALCOHOL (UNII: 172F2WN8DV)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- MICA (UNII: V8A1AW0880)
- ALUMINUM OXIDE (UNII: LMI26O6933)
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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".