NDC 14783-302 Esika Silk Skin
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 14783-302?
What are the uses for Esika Silk Skin?
Which are Esika Silk Skin UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Esika Silk Skin 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)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ZINC STEARATE (UNII: H92E6QA4FV)
- MINERAL OIL (UNII: T5L8T28FGP)
- MICA (UNII: V8A1AW0880)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- PETROLATUM (UNII: 4T6H12BN9U)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CANDELILLA WAX (UNII: WL0328HX19)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".