NDC 13537-125 Cyzone Cy Cover Mat
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd.
- 13537-125 - Cyzone
Product Characteristics
BROWN (C48332 - OVER SAND - BEIGE)
BROWN (C48332 - MIDD CONFIDENTIAL - BEIGE)
Product Packages
NDC Code 13537-125-01
Package Description: 1 TUBE in 1 BAG / 27 g in 1 TUBE
Product Details
What is NDC 13537-125?
What are the uses for Cyzone Cy Cover Mat?
Which are Cyzone Cy Cover Mat UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Cyzone Cy Cover Mat 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- BAMBUSA ARUNDINACEA STEM (UNII: NRA4497HC5)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- IMPERATA CYLINDRICA ROOT (UNII: VYT2JA85NH)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* 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".