NDC 58411-826 Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum Spf 25 Sunscreen 1c0 Cameo
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 58411-826?
What are the uses for Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum Spf 25 Sunscreen 1c0 Cameo?
Which are Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum Spf 25 Sunscreen 1c0 Cameo 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)
Which are Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum Spf 25 Sunscreen 1c0 Cameo 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)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ASCOPHYLLUM NODOSUM (UNII: 168S4EO8YJ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- COCO GLUCOSIDE (UNII: ICS790225B)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BATILOL (UNII: 39YR661C4U)
- BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".