NDC 13537-456 Esika Perfect Match Spf 20 Red Supreme
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
PINK (C48328)
WHITE (C48325 - BEIGE)
RED (C48326)
ORANGE (C48331)
Code Structure Chart
Product Details
What is NDC 13537-456?
What are the uses for Esika Perfect Match Spf 20 Red Supreme?
Which are Esika Perfect Match Spf 20 Red Supreme UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Esika Perfect Match Spf 20 Red Supreme 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:
- CASTOR OIL (UNII: D5340Y2I9G)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CANDELILLA WAX (UNII: WL0328HX19)
- SHEA BUTTER (UNII: K49155WL9Y)
- CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- GLYCERIN (UNII: PDC6A3C0OX)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- .BETA.-SITOSTEROL (UNII: S347WMO6M4)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- PETROLATUM (UNII: 4T6H12BN9U)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
- SUCROSE COCOATE (UNII: 3H18P0UK73)
- MANGANESE VIOLET (UNII: 72M48QQV8Q)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- TALC (UNII: 7SEV7J4R1U)
- D&C RED NO. 6 (UNII: 481744AI4O)
- D&C RED NO. 21 (UNII: 08744Z6JNY)
* 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".