NDC 62839-1640 Nu Skin Ageloc Me
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62839 - Nse Products, Inc.
- 62839-1640 - Nu Skin Ageloc Me
Product Packages
NDC Code 62839-1640-1
Package Description: 1 KIT in 1 CARTON * 12 mL in 1 CARTRIDGE * 12 mL in 1 CARTRIDGE * 12 mL in 1 CARTRIDGE * 28 mL in 1 CARTRIDGE * 28 mL in 1 CARTRIDGE (62839-1617-1)
Product Details
What is NDC 62839-1640?
What are the uses for Nu Skin Ageloc Me?
Which are Nu Skin Ageloc Me UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Nu Skin Ageloc Me 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- RICE GERM (UNII: 7N2B70SFEZ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- 4-TERT-BUTYLCYCLOHEXANOL (UNII: K0H1405S9C)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ALLANTOIN (UNII: 344S277G0Z)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
- SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)
- CORN OIL (UNII: 8470G57WFM)
- NARCISSUS TAZETTA BULB (UNII: K17762966S)
- 7-DEHYDROCHOLESTEROL (UNII: BK1IU07GKF)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- TOCOPHEROL (UNII: R0ZB2556P8)
* 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".