Label: CLEARSKIN PROFESSIONAL DAILY CORRECTING- 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 January 1, 2019

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

  • ACTIVE INGREDIENT

    Active/Medicinal Ingredient
    Salicylic Acid 0.50%..............................

       Purpose
    ...............Acne Treatment

  • INDICATIONS & USAGE

    Uses

    • for the treatment of acne
    • reduces the number of acne blemishes
    • helps clear up most acne blemishes
  • WARNINGS

    Warnings

    For external use only

    When using this product

    • avoid contact with eyes. If product contacts eyes, rinse thoroughly with water.If irritation persists, seek medical attention.
    • discontinue use if excessive skin irritation develops or increases. If irritationpersists, consult a health care practitioner.
    • using other topical acne products at the same time or immediately afterthis product may increase dryness or irritation of the skin. If this occurs,only one product should be used unless directed by  a health care practitioner

    Sunburn Alert: Use only as directed. This product contains an alpha hydroxy acid that may increase your skin’s sensitivity to the sun and particularly the possibility of sunburn. Please limit sun exposure and apply a sunburn protectant while using this product and for a week afterwards.

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

  • DOSAGE & ADMINISTRATION

    Directions

    • cleanse skin thoroughly before applying product
    • apply a thin layer of product to affected areas one to three times daily or as directed by a health care practitioner
    • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to three times daily if needed or as directed by a health care practitioner
    • if bothersome dryness or peeling occurs, reduce application to once a day or every other day
  • INACTIVE INGREDIENT

    Inactive/Non-medicinal
    Ingredients
    WATER/EAU, SD ALCOHOL 40-B, DIMETHICONE, C12-15 ALKYL BENZOATE, KAOLIN, PROPYLENE GLYCOL, CYCLOPENTASILOXANE, CETEARYL ALCOHOL, CETYL ALCOHOL, ETHYLHEXYL
    METHOXYCINNAMATE, STEARYL ALCOHOL, THIODIPROPIONIC ACID, ZINC HEXAPEPTIDE-11, HEXAPEPTIDE-11, GLYCOLIC ACID, PALMITOYL OLIGOPEPTIDE, PALMITOYL TETRAPEPTIDE-7, RETINYL PALMITATE, TRITICUM VULGARE (WHEAT) GERM EXTRACT, CINNAMOMUM ZEYLANICUM BARK EXTRACT, SARCOSINE, TOCOPHEROL, CAPRYLOYL GLYCINE, PVM/MA DECADIENE CROSSPOLYMER, CYCLOHEXASILOXANE, STEARETH-21, CETEARETH-20, DIMETHICONE CROSSPOLYMER, PEG-40 STEARATE, CARBOMER, POLYSORBATE 20, HEXYLENE GLYCOL, ISODODECANE, POLYSORBATE 60, PEG-150 STEARATE, STEARETH-20, GLYCERIN, BUTYLENE GLYCOL, POLYSTYRENE/HYDROGENATED POLYISOPENTENE COPOLYMER, PARFUM/FRAGRANCE, SODIUM HYDROXIDE, DISODIUM EDTA, METHYLPARABEN, PROPYLPARABEN, PHENOXYETHANOL.

  • QUESTIONS

    Questions?
    Call 1-800-FOR-AVON

  • PRINCIPAL DISPLAY PANEL

    image of PDPimage of label

  • INGREDIENTS AND APPEARANCE
    CLEARSKIN  PROFESSIONAL DAILY CORRECTING
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10096-0154
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10096-0154-21 in 1 CARTON11/09/2011
    1NDC:10096-0154-160 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    2NDC:10096-0154-41 in 1 CARTON11/09/2011
    2NDC:10096-0154-315 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D11/09/2011
    Labeler - New Avon LLC (080143520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Fareva Morton Grove, Inc.116752326manufacture(10096-0154)