NDC 82701-001 Belo Sun Expert Tinted Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 82701-001?
What are the uses for Belo Sun Expert Tinted Sunscreen?
Which are Belo Sun Expert Tinted Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Belo Sun Expert Tinted Sunscreen 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:
- APIS MELLIFERA VENOM (UNII: 76013O881M)
- BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)
- NIACINAMIDE (UNII: 25X51I8RD4)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- WATER (UNII: 059QF0KO0R)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- LAUROYL LYSINE (UNII: 113171Q70B)
- POLYMETHYLSILSESQUIOXANE/TRIMETHYLSILOXYSILICATE (UNII: X2PZH4Y6HT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- LEVOMENOL (UNII: 24WE03BX2T)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- C30-45 ALKYL CETEARYL DIMETHICONE CROSSPOLYMER (UNII: 4ZK9VP326R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- AVOBENZONE (UNII: G63QQF2NOX)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CETEARETH-12 (UNII: 7V4MR24V5P)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- EDETATE SODIUM (UNII: MP1J8420LU)
- PEG-80 SORBITAN PALMITATE (UNII: 4NR71FN0IA)
- CYCLOMETHICONE 4 (UNII: CZ227117JE)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
* 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".