Label: IMAGE CLEAR CELL ACNE SPOT TREATMENT- salicylic acid acne gel gel

  • NDC Code(s): 60232-5022-1
  • Packager: Swiss-American CDMO, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2025

If you are a consumer or patient please visit this version.

  • Warnings

    For external use only.  Do not use if you have very sensitive skin.  When using this product, skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time.  If irritation occurs, only use one topical acne medication at a time.  Avoid unnecessary sun exposure and use a sunscreen.  Avoid contact with the eyes, lips and mouth.  Avoid contact with hair and dyed fabrics, which may be bleached by this product.  Skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling.  Irritation may be reduced by using the product less frequently or in a lower concentration.  Stop use and ask a doctor if irritation becomes severe.  If swallowed, get medical help or contact a Poison Control Center right away.

  • Active Ingredients

    Salicylic Acid 2%

  • Purpose

    Acne treatment

  • Use

    For the treatment of acne

  • Directions

    Clean the skin thoroughly before applying this product.  Cover the entire affected area with a thin layer one to three times daily.  Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.  If bothersome dryness or peelig occurs, reduce application to once a day or every other day. 

    Sensitivity Test for a New User: Apply product sparingly to one or two small affected areas during the first 3 days.  If no discomfort occurs, follow the directions stated above.

  • Keep out of reach of children

    Keep out of reach of children

  • Other information

    Store at room temperature

  • Inactive Ingredients

    water, propanediol, butylene glycol, polyacrylate crosspolymer-6, glycerin, dimethyl isosorbide, zinc PCA, melaleuca alfernifolia (tea tree) leaf oil, tasmannia lanceolata fruit/leaf extract, zingiber officinale (ginger) root extract, cinnamomum cassia bark extract, sanguisorba officinalis root extract, laminaria digitata extract, chlorella vulgaris extract, saccharide isomerate, terpineol, alpha-terpinene, trpinolene, pinene, maris aqua, ethylhexylgylcerin, sodium hdyroxide, phenoxyethanol

  • Questions

    Questions? Call 800-796-7546

  • Labeling

    Image Clear Cell UC

  • INGREDIENTS AND APPEARANCE
    IMAGE CLEAR CELL ACNE SPOT TREATMENT 
    salicylic acid acne gel gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60232-5022
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 g  in 1000 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM CARBONATE (UNII: 45P3261C7T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TASMANNIA LANCEOLATA FRUIT (UNII: PNT2HDL13Q)  
    CINNAMOMUM CASSIA BARK (UNII: WS4CQ062KM)  
    ZINGIBER OFFICINALE (GINGER) ROOT OIL (UNII: SAS9Z1SVUK)  
    SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X)  
    LAMINARIA DIGITATA (UNII: 15E7C67EE8)  
    CHLORELLA VULGARIS (UNII: RYQ4R60M02)  
    SACCHARIDE ISOMERATE (UNII: W8K377W98I)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ZINC PCA (UNII: C32PQ86DH4)  
    MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)  
    POLYACRYLATE CROSSPOLYMER-6 (UNII: Q7UI015FF9)  
    Product Characteristics
    Colorbrown (light brown) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60232-5022-114 g in 1 TUBE; Type 0: Not a Combination Product12/11/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00612/11/2025
    Labeler - Swiss-American CDMO, LLC (080170933)
    Registrant - Swiss-American CDMO, LLC (080170933)
    Establishment
    NameAddressID/FEIBusiness Operations
    Swiss-American CDMO, LLC080170933manufacture(60232-5022)