NDC 58411-369 Laura Mercier Tinted Moisturizer Illuminating Broad Spectrum Spf 20 Sunscreen 5n1 Bronze Radiance
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 58411-369?
What are the uses for Laura Mercier Tinted Moisturizer Illuminating Broad Spectrum Spf 20 Sunscreen 5n1 Bronze Radiance?
Which are Laura Mercier Tinted Moisturizer Illuminating Broad Spectrum Spf 20 Sunscreen 5n1 Bronze Radiance 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 Tinted Moisturizer Illuminating Broad Spectrum Spf 20 Sunscreen 5n1 Bronze Radiance 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)
- MICA (UNII: V8A1AW0880)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
- PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- ANHYDROXYLITOL (UNII: 8XWR7NN42F)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- XYLITOL (UNII: VCQ006KQ1E)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALLANTOIN (UNII: 344S277G0Z)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- COPPER GLUCONATE (UNII: RV823G6G67)
- HYDROGENATED OLIVE OIL (UNII: 53839415GI)
- SHEA BUTTER (UNII: K49155WL9Y)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- EDETATE SODIUM (UNII: MP1J8420LU)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- SODIUM ASCORBATE (UNII: S033EH8359)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROUS OXIDE (UNII: G7036X8B5H)
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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".