NDC 60541-8407 Octinoxate
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 60541-8407?
What are the uses for Octinoxate?
Which are Octinoxate UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Octinoxate 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)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K)
- TRIDECYL TRIMELLITATE (UNII: FY36J270ES)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
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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".