Label: DR. C. TUNA SUN 6 SPF TAN AND CARE CARROT- octinoxate oil

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

Drug Label Information

Updated December 9, 2023

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  • Drug Facts

  • Active Ingredients

    Ethylhexyl Methoxycinnamate 3,5%

  • PURPOSE

    Sunscreen

  • Uses

    Helps prevent sunburn.

  • 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 rash occurs.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. 

  • Directions

    Apply liberally 15 minutes before sun exposure – reapply: after 80 minutes of swimming or sweating – immediately after towel drying – at least every two hours.

    Spending time in the sun with a broad spectrum SPF of 6 or higher and other sun protection measures including: - limit time in the sun, especially from 10 a.m. – 2 p.m. – wear long-sleeve shirts, pants, hats and sunglasses – children under 6 months: Ask a doctor Sun Protection Measures:

  • Other information

    Protect this product from excessive heat and direct sun. May stain some fabrics

  • Inactive Ingredients

    Mineral Oil/Paraffinum Liquidum, Fragrance/Parfum, Soybean Oil/Glycine Soja Oil, Daucus Carota Sativa Root Extract, Beta-Carotene, Tocopherol, Coumarin.

  • Questions or Comments? 

    info@farmasius.com 1 786 238 7338

    Monday - Friday (9 a.m - 6 p.m. EST)

  • SPL UNCLASSIFIED SECTION

    Manufactured by: Tan-Alize Kozmetik ve Temizlik Ürünleri San. ve. Tic. A.S. Ömerli Mah. Uran Cad. No: 32 / 34797 Cekmeköy / ISTANBUL 

    Made in TURKEY

    EU REsponsible Person: Farmasi Central Europe S.R.O. Stará Vajnorská Republika. Distributed By: FARMASI US LLC 2315 NW 107 TH AVE, STE 1B 12, DORAL , FL 33172.

  • Package Labeling

    label

  • INGREDIENTS AND APPEARANCE
    DR. C. TUNA SUN 6 SPF TAN AND CARE CARROT 
    octinoxate oil
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74690-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE35 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    MINERAL OIL (UNII: T5L8T28FGP)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    CARROT (UNII: L56Z1JK48B)  
    BETA CAROTENE (UNII: 01YAE03M7J)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    COUMARIN (UNII: A4VZ22K1WT)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74690-002-01115 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/08/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/08/2020
    Labeler - Farmasi US LLC (113303351)
    Establishment
    NameAddressID/FEIBusiness Operations
    TAN-ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI365979587manufacture(74690-002)
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