Label: CLEAR CHOICE BP 8 TOPICAL ACNE- benzoyl peroxide gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 7, 2024

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

  • DRUG FACTS:

  • Active Ingredients

    Benzoyl Peroxide 8%

    Purpose

    Acne Treatment

  • Indications:

    • For the use of Acne
    • Prevents future Acne breakouts
    • Eliminates P-bacteria
  • Warnings:

    For external use only - DO NOT APPLY TO BROKEN SKIN

    - When using this product,

    keep out of eyes. Rinse with water to remove. May bleach colored fabrics. Discontinue use if signs of rash or irritation appear.

    Keep out of reach of children.

    Keep this and all drugs out of reach of children in case of accidental ingestion, contact a Poison Control Center or get medical help.

  • Directions:

    Apply over entire face or affected area. Dryness may occur, start with one daily application and increase as needed or as directed by your skincare professional. Avoid eye contact. Sunblock is recommended.

  • Inactive Ingredients:

    Purified Water, Certified Organic Aloe Vera Gel, Japanese Green Tea Extract, Vegetable Glycerin, Cetearyl Alcohol (and) Ceteareth-20, Benzoyl Peroxide, Caprylic/Capric Triglycerides, Thiotic (Alpha Lipoic) Acid, Cetyl Alcohol, Dexapanthenol (Vitamin B5), Vitamin E Acetate, Lecithin, Retinyl Palmitate (Vitamin A), Sodium Hyaluronate, NaPCA, Extracts of Corn Silk, Alpha Bisabolol (Chamomile), Comfrey Root and Centella Asiatica, Magnesium Ascorbyl Phosphate (Vitamin C), and Grapeseed Extract.

  • Questions or comments?

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  • Label

    Label.jpg

  • INGREDIENTS AND APPEARANCE
    CLEAR CHOICE BP 8 TOPICAL ACNE 
    benzoyl peroxide gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83722-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE80 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    PANTOTHENIC ACID (UNII: 19F5HK2737)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    VITAMIN A (UNII: 81G40H8B0T)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    CHAMOMILE (UNII: FGL3685T2X)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    VITIS VINIFERA SEED (UNII: C34U15ICXA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83722-001-0060 mL in 1 TUBE; Type 0: Not a Combination Product02/07/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugOKM00602/07/2024
    Labeler - Dermastart Inc (146909283)