NDC 11822-1214 Facial Sunscreen With Zinc Spf 50 Daylogic
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 11822-1214?
Which are Facial Sunscreen With Zinc Spf 50 Daylogic UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Facial Sunscreen With Zinc Spf 50 Daylogic 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- COCOA BUTTER (UNII: 512OYT1CRR)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- WATER (UNII: 059QF0KO0R)
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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".