NDC 68828-165 Sunscreen Broad Spectrum Spf 50 Jafra
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68828 - Jafra Cosmetics International
- 68828-165 - Sunscreen Broad Spectrum Spf 50
Product Packages
NDC Code 68828-165-02
Package Description: 1 TUBE in 1 CARTON / 125 mL in 1 TUBE (68828-165-01)
NDC Code 68828-165-04
Package Description: 1 TUBE in 1 CARTON / 200 mL in 1 TUBE (68828-165-03)
Product Details
What is NDC 68828-165?
What are the uses for Sunscreen Broad Spectrum Spf 50 Jafra?
Which are Sunscreen Broad Spectrum Spf 50 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Sunscreen Broad Spectrum Spf 50 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:
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- ALLANTOIN (UNII: 344S277G0Z)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- ARGININE (UNII: 94ZLA3W45F)
- DOCOSANOL (UNII: 9G1OE216XY)
- LEVOMENOL (UNII: 24WE03BX2T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LAUROYL LYSINE (UNII: 113171Q70B)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- MICA (UNII: V8A1AW0880)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PANTHENOL (UNII: WV9CM0O67Z)
- PEG-100 STEARATE (UNII: YD01N1999R)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- 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".