NDC 68479-608 Total Eye Care Spf 15
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What is NDC 68479-608?
What are the uses for Total Eye Care Spf 15?
Which are Total Eye Care Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Total Eye Care Spf 15 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)
- C12-15 ALKYL ETHYLHEXANOATE (UNII: GQJ580CH83)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- THERMUS THERMOPHILUS LYSATE (UNII: 775R692494)
- LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- BETAINE (UNII: 3SCV180C9W)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- PEG-100 STEARATE (UNII: YD01N1999R)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- SEDUM ROSEUM ROOT (UNII: 3S5ITS5ULN)
- LEVOMENOL (UNII: 24WE03BX2T)
- ALLANTOIN (UNII: 344S277G0Z)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- XANTHAN GUM (UNII: TTV12P4NEE)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- TOCOPHEROL (UNII: R0ZB2556P8)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- MICA (UNII: V8A1AW0880)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERROUS OXIDE (UNII: G7036X8B5H)
* 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".