NDC 59779-264 Cvs Revitalift Complete With Spf-15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 59779-264?
What are the uses for Cvs Revitalift Complete With Spf-15?
Which are Cvs Revitalift Complete With Spf-15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Cvs Revitalift Complete With Spf-15 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- TROLAMINE (UNII: 9O3K93S3TK)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- DOCOSANOL (UNII: 9G1OE216XY)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PANTHENOL (UNII: WV9CM0O67Z)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
* 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".