NDC 13537-306 Esika Hydro-nutrative Foundation Spf 13
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BROWN (C48332 - BEIGE 2)
Code Structure Chart
Product Details
What is NDC 13537-306?
What are the uses for Esika Hydro-nutrative Foundation Spf 13?
Which are Esika Hydro-nutrative Foundation Spf 13 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 Hydro-nutrative Foundation Spf 13 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 (UNII: NMQ347994Z)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- TALC (UNII: 7SEV7J4R1U)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- PEA (UNII: W4X7H8GYFM)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- ROSA CENTIFOLIA FLOWER OIL (UNII: H32V31VMWY)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- MANNITOL (UNII: 3OWL53L36A)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- PETROLATUM (UNII: 4T6H12BN9U)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- YEAST (UNII: 3NY3SM6B8U)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- CANDELILLA WAX (UNII: WL0328HX19)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".