NDC 13537-156 Esika Total Sec Ultra Fresh
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation, Ltd.
- 13537-156 - Esika
Product Packages
NDC Code 13537-156-01
Package Description: 50 mL in 1 BOTTLE
Product Details
What is NDC 13537-156?
What are the uses for Esika Total Sec Ultra Fresh?
Which are Esika Total Sec Ultra Fresh UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V)
- ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (Active Moiety)
Which are Esika Total Sec Ultra Fresh 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)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-21 (UNII: 53J3F32P58)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- LEVOMENOL (UNII: 24WE03BX2T)
- TRICLOSAN (UNII: 4NM5039Y5X)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MENTHYL PYRROLIDONE CARBOXYLATE, (-),DL- (UNII: 8P18J856U2)
- EDETATE SODIUM (UNII: MP1J8420LU)
- MENTHOL (UNII: L7T10EIP3A)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- BAMBUSA ARUNDINACEA LEAF (UNII: HW86D1FGSS)
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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".