NDC 67938-3051 Elizabeth Arden Prevage Anti-aging Foundation Broad Spectrum Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 67938-3051?
What are the uses for Elizabeth Arden Prevage Anti-aging Foundation Broad Spectrum Sunscreen Spf 30?
Which are Elizabeth Arden Prevage Anti-aging Foundation Broad Spectrum Sunscreen Spf 30 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 Elizabeth Arden Prevage Anti-aging Foundation Broad Spectrum Sunscreen Spf 30 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 5 (UNII: 0THT5PCI0R)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- MYRISTYL TRISILOXANE (UNII: J7960S4R1T)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- GLYCERIN (UNII: PDC6A3C0OX)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- MICA (UNII: V8A1AW0880)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CARNOSINE (UNII: 8HO6PVN24W)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- FERULIC ACID (UNII: AVM951ZWST)
- HYDROXYDECYL UBIQUINOYL DIPALMITOYL GLYCERATE (UNII: OV1BT2N8RC)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- 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".