NDC 62362-149 Neova Dna Damage Control - Silc Sheer Spf 45
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 62362-149?
What are the uses for Neova Dna Damage Control - Silc Sheer Spf 45?
Which are Neova Dna Damage Control - Silc Sheer Spf 45 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Neova Dna Damage Control - Silc Sheer Spf 45 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:
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- OCTYL STEARATE (UNII: 772Y4UFC8B)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- LUTEIN (UNII: X72A60C9MT)
- ROSEMARY (UNII: IJ67X351P9)
- SQUALANE (UNII: GW89575KF9)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- CARAMEL (UNII: T9D99G2B1R)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
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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".