Label: CLEAR PROOF ACNE SYSTEM- benzoyl peroxide and salicylic acid kit

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 17, 2024

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  • Clarifying Cleansing Gel

    Drug Facts

  • Active ingredient

    Salicylic Acid (2% W/W)

    Purpose

    Acne Medication

  • Uses

    • for the management of acne
    • reduces the number of blackheads and acne pimples
    • helps prevent new acne pimples
  • Warnings

    For external use only

    When using this product

    • 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.

    • avoid contact with the eyes

    Stop use and ask a doctor if

    irritation or sensitivity develops or occurs

    Keep our of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • cleanse skin thoroughly before applying medication
    • cover the entire affected area with a thin layer then rinse thoroughly 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

    arctium lappa root extract, butylene glycol, citric acid, cocamidopropyl betaine, cystoseira amentacea/caespitosa branchycarpa extract, disodium EDTA, DMDM hydantoin, epilobium angustifolium flower/leaf/stem extract, ethylparaben, glycerin, methylparben, phenoxyethanol, propylene glycol, propylparaben, sodium C14-16 olefin sulfonate, sodium chloride, triethanolamine, water

  • Blemish Control Toner

    Drug Facts

  • Active ingredient

    Salicylic Acid (2% W/W)

    Purpose

    Acne Medication

  • Uses

    • for the management of acne
    • reduces the number of blackheads and acne pimples
    • helps prevent new acne pimples
  • Warnings

    For external use only

    When using this product

    • 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.
    • avoid contact with the eyes

    Stop use and ask a doctor if

    irritation or sensitivity develops or increases

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • cleanse the skin thoroughly before applying this product
    • 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., citric acid, diethylhexyl sodium sulfosuccinate, eucalyptus globulus leaf oil, menthol, propylene glycol, simethicone, water

  • Acne Treatment Gel

    Drug Facts

  • Active ingredient

    Benzoyl Peroxide 5%

    Purpose

    Acne Medication

  • Uses

    • for the management of acne
    • dries up acne pimples
    • helps prevent new acne pimples
  • Warnings

    For external use only

    Do not use if you

    • have very sensitive skin
    • are sensitive to benzoyl peroxide

    When using this product

    • 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.
    • avoid unnecessary sun exposure and use a sunscreen
    • avoid contact with the eyes, lips, and mouth
    • avoid contact with hair and dyed fabrics, which may be bleached by this product
    • skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.

    Stop use and ask a doctor if

    irritation becomes severe

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    • cleanse the skin thoroughly before applying this product
    • 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
    • if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.
  • Other information

    • store at 59° F to 86° F
    • expiration date on tube crimp
  • Inactive ingredients

    aesculus hippocastanum (horse chestnut) seed extract, butylene glycol, carbomer, cucumis sativus (cucumber) fruit extract, diethylhexyl sodium sulfosuccinate, disodium EDTA, echinacea purpurea extract, glycerin, poloxamer 182, propylene glycol, silica, sodium hydroxide, water

  • Oil-Free Moisturizer for Acne-Prone Skin

  • INGREDIENTS:

    Water/Eau, Glycerin, Cetearyl Ethylhexanoate, Butylene Glycol, Caprylic/Capric Triglyceride, Glyceryl Stearate, Dimethicone, Isostearyl Alcohol, Stearic Acid, Betaine, Niacinamide, PEG-100 Stearate, Cetyl Alcohol, Cucurbita Pepo (Pumpkin) Fruit Extract, Silybum Marianum Fruit Extract, Tocopheryl Acetate, Lactobacillus/Ganoderma Lucidum (Reishi) Extract/Lentinus Edodes (Truncated), PEG-4 Laurate, Triethanolamine, Xanthan Gum, Carbomer, Disodium EDTA, Iodopropynyl Butylcarbamate, Phenoxyethanol, Diazolidinyl Urea, Sodium Benzoate

  • Principal Display Panel - kit carton

    clear proof acne system

    clarifying cleansing gel salicylic acid acne medication 4.5 OZ. NET WT. / 127 g

    blemish control toner salicylic acid acne medication liquid 5 FL. OZ. / 147 ml

    acne treatment gel benzoyl peroxide acne medication 1 OZ. NET WT. / 28 g

    oil-free moisturizer for acne-prone skin 3 FL. OZ. / 88 ml

    image of kit carton

  • INGREDIENTS AND APPEARANCE
    CLEAR PROOF ACNE SYSTEM 
    benzoyl peroxide and salicylic acid kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51531-8977
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51531-8977-01 in 1 CARTON08/15/2013
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 TUBE 28 g
    Part 21 BOTTLE 147 mL
    Part 31 TUBE 127 g
    Part 41 TUBE 88 mL
    Part 1 of 4
    CLEAR PROOF ACNE TREATMENT  ACNE MEDICATION
    benzoyl peroxide gel
    Product Information
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLOXAMER 182 (UNII: JX0HIX6OAG)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    DOCUSATE SODIUM (UNII: F05Q2T2JA0)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ECHINACEA PURPUREA (UNII: QI7G114Y98)  
    CUCUMBER (UNII: YY7C30VXJT)  
    HORSE CHESTNUT (UNII: 3C18L6RJAZ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    128 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00608/15/2013
    Part 2 of 4
    CLEAR PROOF BLEMISH CONTROL TONER  ACNE MEDICATION
    salicylic acid liquid
    Product Information
    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)  
    ALCOHOL (UNII: 3K9958V90M)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    DOCUSATE SODIUM (UNII: F05Q2T2JA0)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    MENTHOL (UNII: L7T10EIP3A)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1147 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00608/15/2013
    Part 3 of 4
    CLEAR PROOF CLARIFYING CLEANSING GEL  ACNE MEDICATION
    salicylic acid gel
    Product Information
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1127 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00608/15/2013
    Part 4 of 4
    CLEAR PROOF OIL-FREE MOISTURIZER FOR ACNE-PRONE SKIN 
    moisturizing [skin care preparations (creams, lotions, powder, and sprays)]
    Product Information
    Other Ingredients
    Ingredient KindIngredient NameQuantity
    INGRPHENOXYETHANOL (UNII: HIE492ZZ3T)  
    INGRSODIUM BENZOATE (UNII: OJ245FE5EU)  
    INGRWATER (UNII: 059QF0KO0R)  
    INGRGLYCERIN (UNII: PDC6A3C0OX)  
    INGRCETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)  
    INGRBUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    INGRMEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    INGRGLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    INGRDIMETHICONE (UNII: 92RU3N3Y1O)  
    INGRBETAINE (UNII: 3SCV180C9W)  
    INGRSTEARIC ACID (UNII: 4ELV7Z65AP)  
    INGRISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y)  
    INGRPEG-100 STEARATE (UNII: YD01N1999R)  
    INGRNIACINAMIDE (UNII: 25X51I8RD4)  
    INGRDIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    INGRCETYL ALCOHOL (UNII: 936JST6JCN)  
    INGRCARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    INGREDETATE DISODIUM (UNII: 7FLD91C86K)  
    INGR.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    INGRPEG-4 LAURATE (UNII: AYF4VM3N1Z)  
    INGRTROLAMINE (UNII: 9O3K93S3TK)  
    INGRXANTHAN GUM (UNII: TTV12P4NEE)  
    INGRPUMPKIN (UNII: SYW0QUB89Y)  
    INGRMILK THISTLE (UNII: U946SH95EE)  
    INGRIODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    188 mL in 1 TUBE; Type 1: Convenience Kit of Co-Package
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Cosmetic08/15/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00608/15/2013
    Labeler - Mary Kay Inc. (049994452)
    Establishment
    NameAddressID/FEIBusiness Operations
    Port Jervis Laboratories Inc.001535103manufacture(51531-8977)
    Establishment
    NameAddressID/FEIBusiness Operations
    Mary Kay Inc.103978839manufacture(51531-8977)
    Establishment
    NameAddressID/FEIBusiness Operations
    Komplete Group Inc.858820962pack(51531-8977)
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