NDC 62839-1103 Nu Skin Nu Colour Tinted Moisturizer Broad Spectrum Spf 15 Honey
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 62839-1103?
What are the uses for Nu Skin Nu Colour Tinted Moisturizer Broad Spectrum Spf 15 Honey?
Which are Nu Skin Nu Colour Tinted Moisturizer Broad Spectrum Spf 15 Honey 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 Nu Skin Nu Colour Tinted Moisturizer Broad Spectrum Spf 15 Honey 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:
- HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- NYLON-12 (UNII: 446U8J075B)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- CORN OIL (UNII: 8470G57WFM)
- CHROMIC OXIDE (UNII: X5Z09SU859)
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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".