NDC 13537-150 Lbel Effet Parfait Loose Extra-fine Portable
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd
- 13537-150 - Lbel
Product Packages
NDC Code 13537-150-02
Package Description: 1 BOTTLE in 1 BOX / 12 g in 1 BOTTLE (13537-150-01)
Product Details
What is NDC 13537-150?
What are the uses for Lbel Effet Parfait Loose Extra-fine Portable?
Which are Lbel Effet Parfait Loose Extra-fine Portable UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Lbel Effet Parfait Loose Extra-fine Portable 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:
- TALC (UNII: 7SEV7J4R1U)
- STARCH, CORN (UNII: O8232NY3SJ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- KAOLIN (UNII: 24H4NWX5CO)
- ZINC STEARATE (UNII: H92E6QA4FV)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- ISOSTEARYL NEOPENTANOATE (UNII: 411THY156Q)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- MAGNESIUM MYRISTATE (UNII: Z1917F0578)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- PETROLATUM (UNII: 4T6H12BN9U)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- CANDELILLA WAX (UNII: WL0328HX19)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
* 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".