Label: DR. C. TUNA ACNE CLEAR COMPLEXION CLEANSER- salicylic acid gel

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

Drug Label Information

Updated November 5, 2023

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  • Drug Facts

  • ACTIVE INGREDIENT

    Salicylic Acid 2%

    PURPOSE

    Acne Treatment

  • USE

    For the treatment of acne.

  • WARNINGS

    For external use only

    When using this product

    skin irritation and dryness is more likely to occur if you combine this product with other topical acne skincare products. If irritation occurs, only use one topical acne skincare product at a time. Avoid sun exposure and use a sunscreen. Avoid contact with the eyes, lips and mouth. If contact occurs, flush thoroughly with water. Skin irritation may occur, characterized by redness or tingling; if increased, discontinue use and seek medical advice.

    Keep out of reach of children.

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

    Do not use

    if you have very sensitive skin or are sensitive to salicylic acid.

  • DIRECTIONS

    Apply to damp skin. Gently massage over face for 20-30 seconds. Avoid the eye area. Rinse thoroughly with warm water and pat dry. Follow with Acne Pore Purifying Toner.

  • OTHER INFORMATION

    Store at room temperature.

  • INACTIVE INGREDIENTS

    Water/Aqua, Cocomidopropyl Betaine, Ammonium Lauryl Sulfat, Sodium Laureth Sulfate, Propylene Glycol, Decyl Glucoside, PEG-150 Distearate, Disodium Cocoamphodiacetate, Glycolic Acid, Glycerin, Hamamelis Virginiana Water, Dehydroacetic Acid, Benzyl Alcohol, Sodium Benzoate, Potassium Sorbate, Styrene/Acrylates Copolymer, Coco-Glucoside, Salix Alba Bark Water, Tea Tree Oil/Melaleuca Alternifolia Leaf Oil, Tetrasodium EDTA, Menthol.

  • Questions or Comments?

    info@farmasius.com Monday – Friday (9 a.m – 6 p.m. EST) (786) 238-7338 

  • Package Labeling:

    Label2

  • INGREDIENTS AND APPEARANCE
    DR. C. TUNA ACNE CLEAR COMPLEXION CLEANSER 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74690-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    SALIX ALBA BARK VOLATILE OIL (UNII: PW3MX00JXN)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    MENTHOL (UNII: L7T10EIP3A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74690-010-011 in 1 BOX01/20/2021
    1100 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00601/20/2021
    Labeler - Farmasi US LLC (113303351)
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