Label: DR. C. TUNA ACNE PORE PURIFYING TONER- salicylic acid liquid

  • NDC Code(s): 74690-009-01, 74690-009-02
  • Packager: Farmasi US LLC
  • 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 0.5%

    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

    After cleansing, apply to face with a soft cotton ball or pad. Avoid the eye area. Do not rinse. Follow with Acne Blemish Control Serum.

  • OTHER INFORMATION

    Store at room temperature.

  • INACTIVE INGREDIENTS

    Water/Aqua, Alcohol Denat, Propylene Glycol, Polysorbate 20, Glycerin, Butylene Glycol, Hamamelis Virginiana Water, Dehydroacetic Acid, Benzyl Alcohol, Glycolic Acid, Phenoxyethanol, Salix Alba Bark Water, Ethylhexylglycerin.

  • Questions or Comments?

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

  • Package Labeling:

    Label

  • 125mL Package Labeling

    125mL Label pt1125mL Label pt2125mL Inner Label pt2125mL Inner Label pt1

  • INGREDIENTS AND APPEARANCE
    DR. C. TUNA ACNE PORE PURIFYING TONER 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74690-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SALIX ALBA BARK VOLATILE OIL (UNII: PW3MX00JXN)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74690-009-011 in 1 BOX01/20/2021
    1225 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:74690-009-021 in 1 BOX07/25/2021
    2125 mL in 1 BOTTLE; 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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