NDC 65342-0945 Laura Mercier Flawless Skin Mega Moisture Creme Broad Spectrum Spf 15 Sunscreen For Normal/dry Skin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65342 - Gurwitch Products, L.l.c.
- 65342-0945 - Laura Mercier Flawless Skin Mega Moisture Creme Broad Spectrum Spf 15 Sunscreen For Normal/dry Skin
Product Packages
NDC Code 65342-0945-0
Package Description: 50 g in 1 JAR
Product Details
What is NDC 65342-0945?
What are the uses for Laura Mercier Flawless Skin Mega Moisture Creme Broad Spectrum Spf 15 Sunscreen For Normal/dry Skin?
Which are Laura Mercier Flawless Skin Mega Moisture Creme Broad Spectrum Spf 15 Sunscreen For Normal/dry Skin UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Laura Mercier Flawless Skin Mega Moisture Creme Broad Spectrum Spf 15 Sunscreen For Normal/dry Skin 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- EMU OIL (UNII: 344821WD61)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITOL (UNII: 506T60A25R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PETROLATUM (UNII: 4T6H12BN9U)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- UREA (UNII: 8W8T17847W)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALLANTOIN (UNII: 344S277G0Z)
- SODIUM ASCORBATE (UNII: S033EH8359)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ISOPROPYLPARABEN (UNII: A6EOX47QK0)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
* 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".