NDC 13537-482 Cyzone Studio Look Polvos Compactos De Alta Cobertura Con Fps 20 (light 1) - Beige
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd
- 13537-482 - Cyzone Studio Look Polvos Compactos De Alta Cobertura Con Fps 20
Product Packages
NDC Code 13537-482-01
Package Description: 1 TUBE in 1 BOX / 7 g in 1 TUBE
Product Details
What is NDC 13537-482?
What are the uses for Cyzone Studio Look Polvos Compactos De Alta Cobertura Con Fps 20 (light 1) - Beige?
Which are Cyzone Studio Look Polvos Compactos De Alta Cobertura Con Fps 20 (light 1) - Beige UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Cyzone Studio Look Polvos Compactos De Alta Cobertura Con Fps 20 (light 1) - 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:
- MICA (UNII: V8A1AW0880)
- TALC (UNII: 7SEV7J4R1U)
- ZINC STEARATE (UNII: H92E6QA4FV)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PERFLUOROOCTYL TRIETHOXYSILANE (UNII: 814P46684U)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- MAGNESIUM MYRISTATE (UNII: Z1917F0578)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
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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".