NDC 11822-9012 Rite Aid Ultimate Sheer
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 11822-9012?
What are the uses for Rite Aid Ultimate Sheer?
Which are Rite Aid Ultimate Sheer 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 Rite Aid Ultimate Sheer 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DOCOSANOL (UNII: 9G1OE216XY)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PEG-4 LAURATE (UNII: AYF4VM3N1Z)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- ETHYLPARABEN (UNII: 14255EXE39)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
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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".