NDC 62839-1135 Nu Skin Nu Colour Advanced Tinted Moisturizer Broad Spectrum Spf 15 - Ochre
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62839 - Nse Products, Inc.
- 62839-1135 - Nu Skin Nu Colour Advanced Tinted Moisturizer Broad Spectrum Spf 15 - Ochre
Product Packages
NDC Code 62839-1135-1
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 40 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 62839-1135?
What are the uses for Nu Skin Nu Colour Advanced Tinted Moisturizer Broad Spectrum Spf 15 - Ochre?
Which are Nu Skin Nu Colour Advanced Tinted Moisturizer Broad Spectrum Spf 15 - Ochre 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 Advanced Tinted Moisturizer Broad Spectrum Spf 15 - Ochre 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- NYLON-12 (UNII: 446U8J075B)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CHROMIC OXIDE (UNII: X5Z09SU859)
* 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".