NDC 43596-0136 Esika Pro Hydra Smart Hydro-nutritive Foundation Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43596 - Ventura Corporation Limited
- 43596-0136 - Esika Pro Hydra Smart Hydro-nutritive Foundation Spf 15
Product Packages
NDC Code 43596-0136-1
Package Description: 28 mL in 1 BOTTLE
Product Details
What is NDC 43596-0136?
What are the uses for Esika Pro Hydra Smart Hydro-nutritive Foundation Spf 15?
Which are Esika Pro Hydra Smart Hydro-nutritive Foundation Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Esika Pro Hydra Smart Hydro-nutritive Foundation Spf 15 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- SILANEDIOL SALICYLATE (UNII: C054DF30K0)
- PEA (UNII: W4X7H8GYFM)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ISODODECANE (UNII: A8289P68Y2)
- HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)
- STARCH, CORN (UNII: O8232NY3SJ)
- CAPRYLOCAPROYL POLYOXYLGLYCERIDES 8 (UNII: 00BT03FSO2)
- TROMETHAMINE (UNII: 023C2WHX2V)
- OCTYLDODECETH-25 (UNII: F8934HEL3M)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DECYLENE GLYCOL (UNII: S57M60MI88)
- DIMETHICONE 100 (UNII: RO266O364U)
- WATER (UNII: 059QF0KO0R)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- PYRROLIDONE CARBOXYLIC ACID (UNII: 6VT1YZM21H)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
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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".