Label: BLAIR AND JACK ANTI-BUMP ACNE TREATMENT- benzoyl peroxide cream

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

Drug Label Information

Updated June 11, 2024

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  • Drug Facts

  • Active ingredient

    Benzoyl peroxide 5.00%

    Purpose

    Acne Treatment

  • Uses

    • For the treatment of acne and shaving bumps
  • Warnings

    For external use only.

    When using this product

    • Use a sunscreen
    • Avoid contact with the eyes, lips and mouth
    • Avoid contact with hair and dyed fabrics (may be bleached by this product).

    Keep out of reach of children.

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

    If pregnant or breast-feeding,

    ask a health professional before use.

    Do not use if you

    • have very sensitive skin
    • are sensitive to benzoyl peroxide.
  • Directions

    • After cleansing the skin, apply the medication to the affected areas in the morning.
  • Other information

    Protect the product in this container from excessive heat and direct sun.

  • Inactive ingredients

    Allantoin, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aminomethyl Propanol, Aqua (Deionized Water), Behenyl Alcohol, Calendula Officinalis Extract, Camellia Sinensis (Green Tea) Extract, Caprylic/Capric Triglyceride, Carbomer, Cymbopogon Schoenanthus (Lemongrass) Oil, Dimethicone, Dioscorea Villosa (Wild Yam) Extract, Ethylhexylglycerin, Glycerin, Hamamelis Virginiana (Witch Hazel), Hydroxyethylcellulose, Phenoxyethanol, Polyacrylate Crosspolymer-6, Sodium Citrate, Sodium Phytate.

  • Question?

    1-844-970-1256

  • Package Labeling

    Label0

  • INGREDIENTS AND APPEARANCE
    BLAIR AND JACK ANTI-BUMP ACNE TREATMENT 
    benzoyl peroxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84377-489
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE50 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    WATER (UNII: 059QF0KO0R)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    CYMBOPOGON SCHOENANTHUS OIL (UNII: XE7K568ILO)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    PHYTATE SODIUM (UNII: 88496G1ERL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84377-489-001 in 1 BOX06/17/2024
    130 mL in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00606/17/2024
    Labeler - Blair + Jack (209190901)
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