NDC 65342-1381 Laura Mercier Tinted Moisturizer Broad Spectrum Spf 20 Sunscreen - Porcelain
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 65342-1381?
What are the uses for Laura Mercier Tinted Moisturizer Broad Spectrum Spf 20 Sunscreen - Porcelain?
Which are Laura Mercier Tinted Moisturizer Broad Spectrum Spf 20 Sunscreen - Porcelain UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- MERADIMATE (UNII: J9QGD60OUZ)
- MERADIMATE (UNII: J9QGD60OUZ) (Active Moiety)
Which are Laura Mercier Tinted Moisturizer Broad Spectrum Spf 20 Sunscreen - Porcelain 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYOXYL 40 CASTOR OIL (UNII: 4ERD2076EF)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALLANTOIN (UNII: 344S277G0Z)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- SODIUM ASCORBATE (UNII: S033EH8359)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- MICA (UNII: V8A1AW0880)
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[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".