Label: IASO INTENSIVE CLEAR BOOSTER- salicylic acid liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated March 2, 2018

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  • ACTIVE INGREDIENT

    active ingredient: salicylic acid

  • INACTIVE INGREDIENT

    Inactive ingredients: aloe barbadensis leaf juice, water, alcohol, butylene glycol, lactc acid, glycolic acid sodium lactate, propylene glycol, sorbitol, sodium pga, polysorbate 20, methylparaben, xanthan gum, disodium EDTA

  • PURPOSE

    An intensive yet extra-gentle skin re-texturizing formula with an exclusive complex of multi-hydroxy acids and plant extracts, which exfoliate dead cells and speed up the skin’s own shedding cycle. Instantly boosts your skin’s smoothness, clarity and radiance and continuously reduces dullness, uneven texture and minor discolorations.Works precisely where and when needed. On dry skin, whisks away flakes. On oily skin reduces surface oil. It also maximizes the benefits of your other skin care products.

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Use morning and night after cleansing. Apply the desired amount evenly to face and neck

  • WARNINGS

    do not use when you feel itching
    do not swallow
    clean the skin before use

  • DOSAGE & ADMINISTRATION

    In the morning and evening after washing apply a small amount to a cotton pad and gently wipe across your face and neck

  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    IASO INTENSIVE CLEAR BOOSTER 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75847-0003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.003 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALCOHOL (UNII: 3K9958V90M)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    SODIUM LACTATE (UNII: TU7HW0W0QT)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SORBITOL (UNII: 506T60A25R)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75847-0003-135 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product03/12/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/09/2011
    Labeler - IASO Inc (688771690)
    Registrant - IASO Inc (688771690)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kolmar Korea Co., Ltd689512611manufacture(75847-0003)
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