Label: SO TOTALLY CLEAN DEEP PORE CLEANSER- salicylic acid liquid

  • NDC Code(s): 70626-104-21, 70626-104-22
  • Packager: ASPIRE BRANDS INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated October 2, 2023

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  • ACTIVE INGREDIENTS

    SALICYLIC ACID 0.5%

  • PURPOSE

    ACNE TREATMENT

  • USE

    ACNE TREATMENT TO HELP CLEAR UP AND PREVENT NEW ACNE BLEMISHES, BLACKHEADS, AND WHITEHEADS.

  • WARNINGS

    • FOR EXTERNAL USE ONLY.
    • FLAMMABLE - KEEP AWAY FROM OPEN FIRE OR FLAME.
  • WHEN USING

    WHEN USING THIS PRODUCT

    • AVOID CONTACT WITH EYES. IF CONTACT OCCURS, FLUSH THOROUGHLU WITH WATER.
    • 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

    KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

  • DIRECTIONS

    • CLEAN THE SKIN THOROUGHLY BEFORE APPLYING THIS PRODUCT.
    • MOISTEN A COTTON BALL. 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 PEELING OCCURS, REDUCE APPLICATION TO ONCE A DAY OR EVERY OTHER DAY.
  • INACTIVE INGREDIENTS

    ALCOHOL DENAT., WATER, SODIUM PCA, LACTIC ACID, FRAGRANCE, ALLANTOIN, SODIUM CARBONATE, RED 4, YELLOW 5, YELLOW 6.

  • PRINCIPAL DISPLAY PANEL

    60mL_STC_OTC_USA_00664

    200mL_STC_OTC_USA_00564

  • INGREDIENTS AND APPEARANCE
    SO TOTALLY CLEAN DEEP PORE CLEANSER 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70626-104
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    ALLANTOIN (UNII: 344S277G0Z)  
    SODIUM CARBONATE (UNII: 45P3261C7T)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70626-104-21200 mL in 1 BOTTLE; Type 0: Not a Combination Product05/02/2016
    2NDC:70626-104-2260 mL in 1 BOTTLE; Type 0: Not a Combination Product05/17/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D05/02/2016
    Labeler - ASPIRE BRANDS INC (832462811)
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