NDC 62839-0805 Nu Skin Nu Colour Moisturshade Finish Spf 15 Honey Beige
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62839 - Nse Products, Inc.
- 62839-0805 - Nu Skin Nu Colour
Product Packages
NDC Code 62839-0805-1
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 30 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 62839-0805?
What are the uses for Nu Skin Nu Colour Moisturshade Finish Spf 15 Honey Beige?
Which are Nu Skin Nu Colour Moisturshade Finish Spf 15 Honey Beige 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Nu Skin Nu Colour Moisturshade Finish Spf 15 Honey Beige 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- OLEIC ACID (UNII: 2UMI9U37CP)
- STEARIC MONOETHANOLAMIDE (UNII: 03XV449Q24)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- PROPYLENE GLYCOL MONOSTEARATE (UNII: F76354LMGR)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PANTHENOL (UNII: WV9CM0O67Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SQUALENE (UNII: 7QWM220FJH)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- LEVOMENOL (UNII: 24WE03BX2T)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- BARIUM SULFATE (UNII: 25BB7EKE2E)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PEG-12 DIMETHICONE (UNII: ZEL54N6W95)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- TROLAMINE (UNII: 9O3K93S3TK)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".