NDC 42877-002 Skin Effects Brightening Day Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42877 - Diversified Global Technologies Dba Diversified Distribution
- 42877-002 - Skin Effects Brightening Day Spf 50
Product Packages
NDC Code 42877-002-01
Package Description: 28.3 g in 1 BOTTLE
Product Details
What is NDC 42877-002?
What are the uses for Skin Effects Brightening Day Spf 50?
Which are Skin Effects Brightening Day Spf 50 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)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Skin Effects Brightening Day Spf 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:
- WATER (UNII: 059QF0KO0R)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PEG-100 STEARATE (UNII: YD01N1999R)
- SHEA BUTTER (UNII: K49155WL9Y)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- CETETH-20 (UNII: I835H2IHHX)
- STEARETH-20 (UNII: L0Q8IK9E08)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- HEXYLRESORCINOL (UNII: R9QTB5E82N)
- SODIUM OLEATE (UNII: 399SL044HN)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- O-CYMEN-5-OL (UNII: H41B6Q1I9L)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
* 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".