NDC 13537-998 Esika Triple Accion Max Bb Dark Beige
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd
- 13537-998 - Esika Triple Accion Max Bb
Product Packages
NDC Code 13537-998-05
Package Description: 1 TUBE in 1 CARTON / 30 g in 1 TUBE (13537-998-04)
NDC Code 13537-998-06
Package Description: 1 g in 1 PACKET
Product Details
What is NDC 13537-998?
What are the uses for Esika Triple Accion Max Bb Dark Beige?
Which are Esika Triple Accion Max Bb Dark Beige UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Esika Triple Accion Max Bb Dark 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- DIMETHYL ETHER (UNII: AM13FS69BX)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- 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".