NDC 43596-0060 Esika Pro Compact High Definintion And Double Finish Spf 15 Medium 5 - Beige
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43596 - Ventura Corporation Ltd
- 43596-0060 - Esika Pro Compact High Definintion And Double Finish Spf 15
Product Packages
NDC Code 43596-0060-2
Package Description: 1 BOTTLE in 1 BOX / 6 g in 1 BOTTLE (43596-0060-1)
Product Details
What is NDC 43596-0060?
What are the uses for Esika Pro Compact High Definintion And Double Finish Spf 15 Medium 5 - Beige?
Which are Esika Pro Compact High Definintion And Double Finish Spf 15 Medium 5 - Beige 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)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Esika Pro Compact High Definintion And Double Finish Spf 15 Medium 5 - Beige 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:
- MICA (UNII: V8A1AW0880)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- ISOSTEARYL NEOPENTANOATE (UNII: 411THY156Q)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CERAMIDE NP (UNII: 4370DF050B)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- 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".