NDC 68828-757 Jafra Royal Luna Bright Kit
Avobenzone,Homosalate,Octisalate,Octocrylene Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 68828-757?
What are the uses for Jafra Royal Luna Bright Kit?
Which are Jafra Royal Luna Bright Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Jafra Royal Luna Bright Kit 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:
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- LAUROYL LYSINE (UNII: 113171Q70B)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- DOCOSANOL (UNII: 9G1OE216XY)
- ARGININE (UNII: 94ZLA3W45F)
- LEVOMENOL (UNII: 24WE03BX2T)
- SHEA BUTTER (UNII: K49155WL9Y)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALLANTOIN, (+)- (UNII: XDK458E1J9)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- PEG-100 STEARATE (UNII: YD01N1999R)
- DULSE (UNII: 7832HOY4ZQ)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- ROYAL JELLY (UNII: L497I37F0C)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PEG-20 SORBITAN ISOSTEARATE (UNII: X958PZJ9ON)
- COCOA (UNII: D9108TZ9KG)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".