NDC 58875-101 Hard Candy Correction Creme
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 58875-101?
Which are Hard Candy Correction Creme UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Hard Candy Correction Creme 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:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SORBIC ACID (UNII: X045WJ989B)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ISODODECANE (UNII: A8289P68Y2)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- MICA (UNII: V8A1AW0880)
- CHROMIC OXIDE (UNII: X5Z09SU859)
- FERRIC FERROCYANIDE (UNII: TLE294X33A)
- CARMINIC ACID (UNII: CID8Z8N95N)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- STEARETH-2 (UNII: V56DFE46J5)
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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".