Label: BLEMISH CONTROL BAR- salicylic acid soap

  • NDC Code(s): 68726-439-01
  • Packager: CP Skin Health Group, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 9, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Salicylic acid 2%

  • Purpose

    Acne treatment

  • Uses

    • for the treatment of acne
    • helps keep skin clear of new acne pimples, blackheads, or whiteheads
  • Warnings

    For external use only.

    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.

    Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

  • Directions

    • clean the skin thoroughly before applying this product
    • cover the entire affected area with a thin layer and rinse thoroughly 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 peeling occurs, reduce application to once a day or every other day
  • Other information

    • store at room temperature
  • Inactive ingredients

    Pentylene Glycol, Glycerin, Sodium Cocoate, Sodium Palm Kernelate, Sodium Castorate, Water, Sodium Safflowerate, Sorbitan Oleate, Sorbitol, Azelaic Acid, Tsuga Canadensis Leaf Oil, Eucalyptus Globulus Leaf Oil, Glycine Soja (Soybean) Protein, Aloe Barbadensis Leaf Juice Powder, Tocopherol, Glycine Soja (Soybean) Oil.

  • Questions?

    Please call 877.722.7546

  • PRINCIPAL DISPLAY PANEL - 90 g Jar Box

    PCA skin®

    blemish control bar

    salicylic acid acne treatment

    01 | cleanse

    3.2 oz (90 g)

    PRINCIPAL DISPLAY PANEL - 90 g Jar Box
  • INGREDIENTS AND APPEARANCE
    BLEMISH CONTROL BAR 
    salicylic acid soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68726-439
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM COCOATE (UNII: R1TQH25F4I)  
    SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
    SODIUM CASTORATE (UNII: 6PAR8M5DCK)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM SAFFLOWERATE (UNII: UHG9F87J7K)  
    SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
    SORBITOL (UNII: 506T60A25R)  
    AZELAIC ACID (UNII: F2VW3D43YT)  
    TSUGA CANADENSIS LEAF OIL (UNII: Q1S51LGQ0G)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    SOY PROTEIN (UNII: R44IWB3RN5)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    Product Characteristics
    ColorBROWN (Pale Beige) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68726-439-011 in 1 BOX04/22/2016
    190 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM00604/22/2016
    Labeler - CP Skin Health Group, Inc. (611921669)
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