NDC 50390-707 Peter Island Ultimate Sheer Dry Touch Sunscreen Spf 70
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50390 - Amway Corp.
- 50390-707 - Peter Island Ultimate Sheer Dry Touch Sunscreen
Product Packages
NDC Code 50390-707-12
Package Description: 85 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 50390-707?
What are the uses for Peter Island Ultimate Sheer Dry Touch Sunscreen Spf 70?
Which are Peter Island Ultimate Sheer Dry Touch Sunscreen Spf 70 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Peter Island Ultimate Sheer Dry Touch Sunscreen Spf 70 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)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- TETRASILANE (UNII: OI9DXJ0BL4)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- CHLORPHENESIN (UNII: I670DAL4SZ)
* 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".