NDC 58892-722 Solar Protection Formula Spf 60 Tinted Concealer - (honey) Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 58892-722?
What are the uses for Solar Protection Formula Spf 60 Tinted Concealer - (honey) Sunscreen?
Which are Solar Protection Formula Spf 60 Tinted Concealer - (honey) Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Solar Protection Formula Spf 60 Tinted Concealer - (honey) Sunscreen 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:
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- .BETA.-CAROTENE (UNII: 01YAE03M7J)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- CARAMEL (UNII: T9D99G2B1R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- ISOPROPYLPARABEN (UNII: A6EOX47QK0)
- LINOLEAMIDOPROPYL DIMETHYLAMINE (UNII: W142CF4WLF)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MARITIME PINE (UNII: 50JZ5Z98QY)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- TALC (UNII: 7SEV7J4R1U)
- TOCOPHEROL (UNII: R0ZB2556P8)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- WATER (UNII: 059QF0KO0R)
* 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".