NDC 68828-500 Jafra Royal Jelly Revitalize
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What is NDC 68828-500?
What are the uses for Jafra Royal Jelly Revitalize?
Which are Jafra Royal Jelly Revitalize 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 Jelly Revitalize 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:
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- KIWI FRUIT OIL (UNII: 66086CWP3Q)
- ALCOHOL (UNII: 3K9958V90M)
- ALLANTOIN (UNII: 344S277G0Z)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- ARGININE (UNII: 94ZLA3W45F)
- DOCOSANOL (UNII: 9G1OE216XY)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- LEVOMENOL (UNII: 24WE03BX2T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SHEA BUTTER (UNII: K49155WL9Y)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- COCONUT (UNII: 3RT3536DHY)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- LAUROYL LYSINE (UNII: 113171Q70B)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- MORINGA OLEIFERA LEAF (UNII: 4WET1AWO9B)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)
- ROYAL JELLY (UNII: L497I37F0C)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- WATER (UNII: 059QF0KO0R)
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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".