NDC 14783-176 Esika Pro Natural Mattifying Foundation Adaptable To Your Skin Tone Spf 20 Claro 1/beige
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14783 - Ventura International Ltd
- 14783-176 - Esika Pro Natural Mattifying Foundation Adaptable To Your Skin Tone Spf 20
Product Packages
NDC Code 14783-176-02
Package Description: 1 BOTTLE in 1 BOX / 30 g in 1 BOTTLE (14783-176-01)
Product Details
What is NDC 14783-176?
What are the uses for Esika Pro Natural Mattifying Foundation Adaptable To Your Skin Tone Spf 20 Claro 1/beige?
Which are Esika Pro Natural Mattifying Foundation Adaptable To Your Skin Tone Spf 20 Claro 1/beige 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 Natural Mattifying Foundation Adaptable To Your Skin Tone Spf 20 Claro 1/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:
- WATER (UNII: 059QF0KO0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ISODODECANE (UNII: A8289P68Y2)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- SILANEDIOL SALICYLATE (UNII: C054DF30K0)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TROMETHAMINE (UNII: 023C2WHX2V)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC; 3000 MW) (UNII: J2S07SB0YL)
- MILK THISTLE (UNII: U946SH95EE)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- 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".