Label: YS SOLUTION AC CONTROL SKIN REGULAR MILD- salicylic acid liquid

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

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated January 17, 2018

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  • ACTIVE INGREDIENT

    active ingredient: salicylic acid

  • INACTIVE INGREDIENT

    Water, Alchol, Butylene Glycol, Magnolol, Salicylic Acid, Arginine, Perfume, Allantoin, Totarol, Bisabolol, Dipotassium, lycyrrhizate, Murdania Keisak Extract, Chlorella Vulgaris Extract, Hammamelis Virginiana(Witch hazel) Extract, Zinc PCA, Houttuynia Cordata Extract, Aloe Barbadensis Leaf Extract

  • PURPOSE

    helps to clear dead cells and sebum that may block skin pores

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    brush your teeth by putting appropriate amount of tooth paste

  • WARNINGS

    for external use only
    avoid contact with eyes
    do not swallow

  • DOSAGE & ADMINISTRATION

    Apply Proper Amount of the toner on the skin.

  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    YS SOLUTION AC CONTROL SKIN REGULAR MILD 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76340-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.47 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ARGININE (UNII: 94ZLA3W45F)  
    ALLANTOIN (UNII: 344S277G0Z)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    CHLORELLA VULGARIS (UNII: RYQ4R60M02)  
    WITCH HAZEL (UNII: 101I4J0U34)  
    ZINC (UNII: J41CSQ7QDS)  
    HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76340-0001-160 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product01/01/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/10/2011
    Labeler - Ajou Medics Co., Ltd (688796473)
    Registrant - Ajou Medics Co., Ltd (688796473)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ajou Medics Co., Ltd688796473manufacture(76340-0001)