Label: DR. C. TUNA RESURFACE ESSENTIAL DAY CREAM- homosalate, octinoxate, octocrylene, avobenzone cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 5, 2023

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  • Drug Facts:

  • Active Ingredient:

    Homosalate 7% Ethylhexyl Methoxycinnamate 5% Octocrylene 5% Butyl Methoxydibenzoylmethane 2%


    Purpose

    Sunscreen

  • Use:

    Helps to moisturize and protect the skin from sun damage.

  • Warnings:

    For external use only.

    Do not use

    on damaged or broken skin.

    When using this product

    keep out of eyes. Rinse with water to remove.

    Stop use and ask doctor if

    skin irritation develops when using this product.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions:

    Directions: Use daily, every morning 15 minutes before sun exposure. Take enough amounts with the enclosed spatula on your hands; gently apply on clean face and neck.

  • 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.

  • Questions or Comments?

    info@farmasius.com (833) 432-7627

    Monday – Friday (9 a.m – 9 p.m. EST)

  • Package Labeling:

    Label4

  • INGREDIENTS AND APPEARANCE
    DR. C. TUNA RESURFACE ESSENTIAL DAY CREAM 
    homosalate, octinoxate, octocrylene, avobenzone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74690-016
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE70 mg  in 1 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE50 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE50 mg  in 1 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74690-016-011 in 1 BOX07/25/2021
    150 mL in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02007/25/2021
    Labeler - Farmasi US LLC (113303351)
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