Label: DR. C. TUNA RESURFACE ESSENTIAL DAY CREAM SPF 30- homosalate, octinoxate, octocrylene, avobenzone kit
- NDC Code(s): 74690-025-00, 74690-026-00
- Packager: Farmasi US LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 5, 2023
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INACTIVE INGREDIENTS:
Water/Aqua, Cetyl Alcohol, Dicaprylyl Carbonate, Caprylic/Capric Triglyceride, Cichorium Intybus Leaf Extract, Hexylene Glycol, Caprylyl Glycol, Glyceryl Stearate SE, Phenoxyethanol, Cetyl Palmitate, Hexyldecanol, Hexyldecyl Laurate, Sodium Stearoyl Glutamate, Glycerin, Sodium Polyacrylate, Helianthus Annuus Seed Oil, Chlorella Vulgaris Extract, Rosmarinus Officinalis Leaf Extract, Niacinamide, Polymethylsilsesquioxane, Disodium EDTA, Xanthan Gum, Ethylhexylglycerin.
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INGREDIENTS AND APPEARANCE
DR. C. TUNA RESURFACE ESSENTIAL DAY CREAM SPF 30
homosalate, octinoxate, octocrylene, avobenzone kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74690-025 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74690-025-00 1 in 1 KIT 08/15/2021 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 PACKET 2.5 mL Part 1 of 1 DR. C. TUNA LUMI RADIANCE BRIGHTENING CREAM 22 SPF
homosalate, octinoxate, octocrylene, avobenzone creamProduct Information Item Code (Source) NDC:74690-026 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 70 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETYL ALCOHOL (UNII: 936JST6JCN) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CHICORY LEAF (UNII: WBQ249COFR) HEXYLENE GLYCOL (UNII: KEH0A3F75J) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) PHENOXYETHANOL (UNII: HIE492ZZ3T) CETYL PALMITATE (UNII: 5ZA2S6B08X) HEXYLDECANOL (UNII: 151Z7P1317) HEXYLDECYL LAURATE (UNII: 0V595C1P6M) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) GLYCERIN (UNII: PDC6A3C0OX) SUNFLOWER OIL (UNII: 3W1JG795YI) CHLORELLA VULGARIS (UNII: RYQ4R60M02) ROSEMARY (UNII: IJ67X351P9) NIACINAMIDE (UNII: 25X51I8RD4) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) XANTHAN GUM (UNII: TTV12P4NEE) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74690-026-00 2.5 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/15/2021 Labeler - Farmasi US LLC (113303351)