NDC 82736-014 Body Sunscreen Fps 50
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 82736-014?
Which are Body Sunscreen Fps 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- 3-HEXYLOXYPROPYLENE GLYCOL (UNII: 3485P35DA4)
- 3-HEXYLOXYPROPYLENE GLYCOL (UNII: 3485P35DA4) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- PROPYLENE GLYCOL 1-OLEATE (UNII: 476821E6GS)
- PROPYLENE GLYCOL 1-OLEATE (UNII: 476821E6GS) (Active Moiety)
Which are Body Sunscreen Fps 50 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:
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- AVOBENZONE (UNII: G63QQF2NOX)
- BENZOPHENONE-2 (UNII: PRR8K3H9VN)
- MYRISTOYL PENTAPEPTIDE-4 (UNII: PMA59A699X)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYL OXOACETATE (UNII: AH46A7531R)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- ARNICA CORDIFOLIA FLOWER (UNII: JCG1OSZ7A8)
- SALVIA APIANA LEAF (UNII: Z29Z21AHMP)
- ARNICA CHAMISSONIS FLOWER (UNII: 88WK5I8R3L)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- SILICON (UNII: Z4152N8IUI)
- HOMOSALATE (UNII: V06SV4M95S)
- ENZACAMENE (UNII: 8I3XWY40L9)
- OCTINOXATE (UNII: 4Y5P7MUD51)
What is the NDC to RxNorm Crosswalk for Body Sunscreen Fps 50?
- RxCUI: 415924 - salicylic acid 10 % Topical Gel
- RxCUI: 415924 - salicylic acid 0.1 MG/MG Topical Gel
* Please review the disclaimer below.
[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".