Label: CLEARSKIN  PROFESSIONAL DAILY CORRECTING- salicylic acid  lotion 

  • Label RSS
  • NDC Code(s): 10096-0154-1, 10096-0154-2, 10096-0154-3, 10096-0154-4
  • Packager: Avon Products, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 02/13

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  • ACTIVE INGREDIENT

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

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

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  • INDICATIONS & USAGE

    Uses

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

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  • 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
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  • 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.

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  • QUESTIONS

    Questions?
    Call 1-800-FOR-AVON

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  • INGREDIENTS AND APPEARANCE
    CLEARSKIN   PROFESSIONAL DAILY CORRECTING
    salicylic acid lotion
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:10096-0154
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALICYLIC ACID (SALICYLIC ACID ) SALICYLIC ACID 5 mg  in 1 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:10096-0154-2 1 in 1 CARTON
    1 NDC:10096-0154-1 60 mL in 1 BOTTLE, PUMP
    2 NDC:10096-0154-4 1 in 1 CARTON
    2 NDC:10096-0154-3 15 mL in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333D 11/09/2011
    Labeler - Avon Products, Inc. (001468693)
    Establishment
    Name Address ID/FEI Business Operations
    Avon Products, Inc. 005149471 manufacture(10096-0154)
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