NDC 13537-996 Esika Triple Accion Max Bb Crema Facial Perfeccionadora Con Color Fps 30 6 Beneficios En 1 Claro (beige)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd
- 13537-996 - Esika Triple Accion Max Bb Crema Facial Perfeccionadora Con Color Fps 30 6 Beneficios En 1
Product Packages
NDC Code 13537-996-02
Package Description: 1 TUBE in 1 BOX / 30 g in 1 TUBE (13537-996-01)
Product Details
What is NDC 13537-996?
What are the uses for Esika Triple Accion Max Bb Crema Facial Perfeccionadora Con Color Fps 30 6 Beneficios En 1 Claro (beige)?
Which are Esika Triple Accion Max Bb Crema Facial Perfeccionadora Con Color Fps 30 6 Beneficios En 1 Claro (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 Triple Accion Max Bb Crema Facial Perfeccionadora Con Color Fps 30 6 Beneficios En 1 Claro (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)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
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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".