Label: DAILY ACNE CONTROL CLEANSER- benzoyl peroxide cream

  • Category: HUMAN OTC DRUG LABEL

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 March 12, 2021

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  • Active ingredient

    Benzoyl peroxide 10%

  • Purpose

    Acne medication

  • use

    for the treatment of acne

  • 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 bleaced by this product
    • skin irritation may occur, characterized by redness, burning, itching, peeling or possible 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.  Avoid contact with eyes.  If contact occurs, flush thoroughly with water.

  • Directions

    • wet face. Gently massage all over face for 20-30 seconds avoiding the eyes.   Rinse thoroughly and pat dry.
    • 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 daily 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
    • Sensitivity Test for a New User.  Apply product sparingly to one or two small affected areas, during the first 3 days.  If no discomfort occurs, follow the directions stated above.
  • Other information

    • keep tightly closed
    • store at room temperature (59⁰-77⁰)
  • Inactive ingredients

    water, cetyl alcohol, petrolatum, acrylates/C10-30 alkyl acrylate crosspolymer, zinc lactate, steareth-2, glycerin, potassium cetyl phosphate, xanthan gum, benzyl alcohol, fragrance, disodium EDTA, laureth-4, BHT, sodium hydroxide, lactic acid, menthol

  • Questions?

    1-800-632-6900

  • Disclaimer

    CLEAN & CLEAR CONTINUOUS CONTROL are registered trademarks of Johnson & Johnson, New Brunswick, New Jersey 08933.  Johnson & Johnson is not affiliated with The Kroger Co. or this product.

  • Adverse Reactions Section

    Quailty Guarantee 800.632.6900  www.kroger.com

    Distributed by the Kroger Co., Cincinnati, Ohio 45202

    264.005/264AI rev1

  • principal display panel

    Compare to CLEAN & CLEAR

    CONTINUOUS CONTROL

    Acne Cleanser

    care

    CLARIFY

    Let's be CLEAR

    Daily Acne Control Cleanser

    10% Benzoyl Peroxide Acne Medication

    Keeps Fighting Acne After You Wash

    Kroger

    NET WT 5 oz (141 g)

    image description

  • INGREDIENTS AND APPEARANCE
    DAILY ACNE CONTROL CLEANSER 
    benzoyl peroxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-264
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE104 mg  in 10 g
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    ZINC LACTATE (UNII: 2GXR25858Y)  
    STEARETH-2 (UNII: V56DFE46J5)  
    glycerin (UNII: PDC6A3C0OX)  
    POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    LAURETH-4 (UNII: 6HQ855798J)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    MENTHOL (UNII: L7T10EIP3A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30142-264-56141 g in 1 TUBE; Type 0: Not a Combination Product08/18/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D08/18/2014
    Labeler - Kroger Inc (006999528)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(30142-264)