NDC 14783-076 Esika Pro Instant Perfection 3 En 1 Face Refining Foundation Spf 25 Medio 3 - Beige
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14783 - Ventura International Ltd
- 14783-076 - Esika Pro Instant Perfection 3 En 1 Face Refining Foundation Spf 25
Product Packages
NDC Code 14783-076-02
Package Description: 1 TUBE in 1 BOX / 3 g in 1 TUBE (14783-076-01)
Product Details
What is NDC 14783-076?
What are the uses for Esika Pro Instant Perfection 3 En 1 Face Refining Foundation Spf 25 Medio 3 - Beige?
Which are Esika Pro Instant Perfection 3 En 1 Face Refining Foundation Spf 25 Medio 3 - 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 Instant Perfection 3 En 1 Face Refining Foundation Spf 25 Medio 3 - 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:
- ISODODECANE (UNII: A8289P68Y2)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- WATER (UNII: 059QF0KO0R)
- STARCH, CORN (UNII: O8232NY3SJ)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BENTONITE (UNII: A3N5ZCN45C)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- SILANEDIOL SALICYLATE (UNII: C054DF30K0)
- OLIVE OIL DECYL ESTERS (UNII: 3AQ222F18X)
- TROMETHAMINE (UNII: 023C2WHX2V)
- LAURETH-12 (UNII: OAH19558U1)
- CERAMIDE NP (UNII: 4370DF050B)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
- SQUALENE (UNII: 7QWM220FJH)
- CHLORELLA VULGARIS (UNII: RYQ4R60M02)
- SEA SALT (UNII: 87GE52P74G)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- MICA (UNII: V8A1AW0880)
* 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".