NDC 20151-105 Lightening High Sun Protection Cream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 20151-105?
What are the uses for Lightening High Sun Protection Cream?
Which are Lightening High Sun Protection Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Lightening High Sun Protection Cream 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:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SOYBEAN (UNII: L7HT8F1ZOD)
- CETETH-20 (UNII: I835H2IHHX)
- STEARETH-20 (UNII: L0Q8IK9E08)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- OCTISALATE (UNII: 4X49Y0596W)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PEG-75 STEARATE (UNII: OT38R0N74H)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- XANTHAN GUM (UNII: TTV12P4NEE)
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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".