NDC 62296-7866 Ulta Sun Dry Touch Spf 55
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62296 - Ulta
- 62296-7866 - Ulta Sun Dry Touch Spf 55
Product Packages
NDC Code 62296-7866-4
Package Description: 147 g in 1 BOTTLE
Product Details
What is NDC 62296-7866?
What are the uses for Ulta Sun Dry Touch Spf 55?
Which are Ulta Sun Dry Touch Spf 55 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 Ulta Sun Dry Touch Spf 55 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)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
- DOCOSANOL (UNII: 9G1OE216XY)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- PEG-4 DILAURATE (UNII: KCR71CW036)
- PEG-4 LAURATE (UNII: AYF4VM3N1Z)
- XANTHAN GUM (UNII: TTV12P4NEE)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POLYETHYLENE GLYCOL 200 (UNII: R95B8J264J)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ETHYLPARABEN (UNII: 14255EXE39)
- 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".