NDC 57627-117 Ultra Light Sunscreen Broad Spectrum Spf 50 Merle Norman
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57627 - Merle Norman Cosmetics
- 57627-117 - Ultra Light Sunscreen Broad Spectrum Spf 50
Product Packages
NDC Code 57627-117-02
Package Description: 1 TUBE in 1 CARTON / 113 g in 1 TUBE (57627-117-01)
NDC Code 57627-117-04
Package Description: 1 TUBE in 1 CARTON / 28 g in 1 TUBE (57627-117-03)
Product Details
What is NDC 57627-117?
What are the uses for Ultra Light Sunscreen Broad Spectrum Spf 50 Merle Norman?
Which are Ultra Light Sunscreen Broad Spectrum Spf 50 Merle Norman UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Ultra Light Sunscreen Broad Spectrum Spf 50 Merle Norman 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- GLYCERIN (UNII: PDC6A3C0OX)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BIS-ETHYLHEXYL HYDROXYDIMETHOXY BENZYLMALONATE (UNII: 7D4Q5YJ8NV)
- POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
* 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".