Label: SALICYLIC WASH- salicylic acid lotion

  • NDC Code(s): 70764-102-16, 70764-102-56
  • Packager: CONTROL CORRECTIVE SKINCARE 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 September 22, 2023

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  • ACTIVE INGREDIENTS

    SALICYLIC ACID (2.0%)

  • PURPOSE

    ACNE TREATMENT

  • USE

    THIS GENTLE FOAMING CLEANSER WORKS TO SMOOTH AND EXFOLIATE DEAD SKIN BUILDUP. MAY BE USED DAILY OR AS DIRECTED BY YOUR SKINCARE SPECIALIST.

  • WARNINGS

    AVOID EYE AREA. DISCONTINUE USE IF IRRITATION OCCURS. DO NOT USE IF ALLERGIC TO ASPERIN.

  • DIRECTIONS

    APPLY A SMALL AMOUNT TO PRE-MOISTENED FINGERS AND LIGHTLY MASSAGE TO AFFECTED AREAS. RINSE WITH TEPID WATER. MAY BE USED ONCE OR TWICE DAILY DEPENDING ON SKIN TYPE.

  • INACTIVE INGREDIENTS

    WATER, AMMONIUM LAURETH SULFATE, AMMONIUM LAURYL SULFATE, COCAMIDOPROPYL BETAINE, ALOE BARBADENSIS LEAF JUICE, GLYCOL STEARATE, SODIUM COCOYL ISETHIONATE, SODIUM LAUROAMPHOACETATE, PHENOXYETHANOL, CHAMOMILE RECUTITA (MATRICARIA) FLOWER EXTRACT, METHYLISOTHIAZOLINONE.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • QUESTIONS OR COMMENTS

    WWW.CONTROLCORRECTIVE.COM

    TOLL FREE 1-866-290-4290   MADE IN USA

  • PRINCIPAL DISPLAY PANEL

    01b UC_Salicylic Wash 2 percent

  • INGREDIENTS AND APPEARANCE
    SALICYLIC WASH 
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70764-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
    SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)  
    SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CHAMOMILE (UNII: FGL3685T2X)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70764-102-561 in 1 BOX06/09/2016
    1NDC:70764-102-16198 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D06/09/2016
    Labeler - CONTROL CORRECTIVE SKINCARE INC (023999357)
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