Label: THAYERS BLEMISH CLEARING BALM- salicylic acid lotion

  • 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 February 21, 2021

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  • ACTIVE INGREDIENT

    active ingredients

  • DOSAGE & ADMINISTRATION

    dosage & administration

  • WARNINGS

    warnings

  • INACTIVE INGREDIENT

    inactive ingredients

  • INDICATIONS & USAGE

    indications & usage

  • PURPOSE

    purpose

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PRINCIPAL DISPLAY PANEL

    package label principal

  • INGREDIENTS AND APPEARANCE
    THAYERS BLEMISH CLEARING BALM 
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60717-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.02 g
    Inactive Ingredients
    Ingredient NameStrength
    EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CARRAGEENAN (UNII: 5C69YCD2YJ)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    WATER (UNII: 059QF0KO0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60717-011-041 in 1 TUBE; Type 0: Not a Combination Product02/22/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D02/22/2021
    Labeler - RNA PHARMA, LLC (079103999)
    Establishment
    NameAddressID/FEIBusiness Operations
    RNA PHARMA, LLC079103999manufacture(60717-011)