NDC 58892-265 Solar Protection Formula Spf 65 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58892 - Fallien Cosmeceuticals, Ltd.
- 58892-265 - Solar Protection Formula Spf 65
Product Packages
NDC Code 58892-265-59
Package Description: 1 BOTTLE in 1 CARTON / 58.8 mL in 1 BOTTLE
Product Details
What is NDC 58892-265?
What are the uses for Solar Protection Formula Spf 65 Sunscreen?
Which are Solar Protection Formula Spf 65 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Solar Protection Formula Spf 65 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:
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- 5-BROMO-5-NITRO-1,3-DIOXANE (UNII: U184I9QBNM)
- .BETA.-CAROTENE (UNII: 01YAE03M7J)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- ISOPROPYLPARABEN (UNII: A6EOX47QK0)
- LINOLEAMIDOPROPYL DIMETHYLAMINE (UNII: W142CF4WLF)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MARITIME PINE (UNII: 50JZ5Z98QY)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- TALC (UNII: 7SEV7J4R1U)
- TOCOPHEROL (UNII: R0ZB2556P8)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- WATER (UNII: 059QF0KO0R)
* 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".