NDC 14783-011 Lbel Effet Parfait
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 14783-011?
What are the uses for Lbel Effet Parfait?
Which are Lbel Effet Parfait 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 Effet Parfait 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:
- OCTYLDODECANOL (UNII: 461N1O614Y)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CANDELILLA WAX (UNII: WL0328HX19)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SHEA BUTTER (UNII: K49155WL9Y)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- WATER (UNII: 059QF0KO0R)
- PETROLATUM (UNII: 4T6H12BN9U)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- STARCH, CORN (UNII: O8232NY3SJ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
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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".