NDC 14783-661 Lbel Couler Luxe Supreme Xp Sublime, Orange, Sobriete
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14783 - Ventura International, Limited
- 14783-661 - Lbel Couler Luxe Supreme Xp
Product Packages
NDC Code 14783-661-12
Package Description: 3 TRAY in 1 KIT / .7 g in 1 TRAY (14783-661-11)
Product Details
What is NDC 14783-661?
What are the uses for Lbel Couler Luxe Supreme Xp Sublime, Orange, Sobriete?
Which are Lbel Couler Luxe Supreme Xp Sublime, Orange, Sobriete 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 Couler Luxe Supreme Xp Sublime, Orange, Sobriete 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)
- CERESIN (UNII: Q1LS2UJO3A)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CANDELILLA WAX (UNII: WL0328HX19)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- MICA (UNII: V8A1AW0880)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ARACHIDYL PROPIONATE (UNII: QV5DAH3MSB)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ETHYL LINOLEATE (UNII: MJ2YTT4J8M)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- D&C RED NO. 6 (UNII: 481744AI4O)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- D&C RED NO. 21 (UNII: 08744Z6JNY)
- D&C RED NO. 17 (UNII: ND733RX3JN)
- OLEYL ALCOHOL (UNII: 172F2WN8DV)
- TALC (UNII: 7SEV7J4R1U)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
* 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".