NDC 68828-242 Royal Jelly Kit Jafra
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 68828-242?
What are the uses for Royal Jelly Kit Jafra?
Which are Royal Jelly Kit Jafra 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 Royal Jelly Kit Jafra 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)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- LAUROYL LYSINE (UNII: 113171Q70B)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- DOCOSANOL (UNII: 9G1OE216XY)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- LEVOMENOL (UNII: 24WE03BX2T)
- ROYAL JELLY (UNII: L497I37F0C)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- COCONUT (UNII: 3RT3536DHY)
- MORINGA OLEIFERA LEAF (UNII: 4WET1AWO9B)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALLANTOIN (UNII: 344S277G0Z)
- ARGININE (UNII: 94ZLA3W45F)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CHICORY ROOT (UNII: 090CTY533N)
- KAPPAPHYCUS ALVAREZII (UNII: T479H08K2O)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- HYDROXYCITRONELLOL (UNII: R0B4U2I48W)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- LINALOOL, (+)- (UNII: F4VNO44C09)
* 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".