Label: 5% BENZOYL PEROXIDE FOLLICULITIS CREAM cream

  • NDC Code(s): 84558-026-01
  • Packager: GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 16, 2026

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

  • Active Ingredient(s)

    Benzoyl peroxide 5%

  • Purpose

    Topical antibacterial

  • Use

    Treats and helps clear mild folliculitis and acne vulgaris (pimples,
    whiteheads, and blackheads) by penetrating pores to help reduce
    acne-causing bacteria, reduce redness and inflammation, and help
    prevent new blemishes.

  • Warnings

    For external use only.

  • Do not use

    Do not use if you are sensitive to benzoyl peroxide.

  • WHEN USING

    .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 swelling. Reduce frequency of use if irritation occurs.

  • STOP USE

    . irritation becomes severe.
    . no improvement is seen after 6 weeks of consistent use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact
    Poison Control right away.

  • Directions

    Clean the skin thoroughly before applying. Apply a thin layer to affected
    areas 1 to 3 times daily. Start with once daily, gradually increase to 2-3
    times if needed. If dryness or peeling occurs, reduce to once daily or
    every other day.

  • Other information

    Store at 20°-25°C(68°-77°F). Do not use if the carton or inner seal is broken.

  • Inactive ingredients

    Water, Glycerin, C12-15 Alkyl Benzoate, Propylene Glycol, Glyceryl
    Stearate, Cetearyl Alcohol, Squalane, Aloe Barbadensis Leaf Juice,
    Dimethicone, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate
    Copolymer, Phenoxyethanol, Panthenol, PEG-100 Stearate,
    Polysorbate 80, Magnesium Aluminum Silicate, Ceramide NP,Sodium
    Hydroxide, Allantoin, Scutellaria Baicalensis Root Extract, Forsythia
    Suspensa Fruit Extract, Portulaca Oleracea Extract, Magnolia Officinalis
    Bark Extract,Calendula Officinalis Flower Extract, Melaleuca Alternifolia
    (Tea Tree) Leaf Oil, Menthy| Lactate, Ethylhexylglycerin, Disodium EDTA

  • Package Label - Principal Display Panel

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  • INGREDIENTS AND APPEARANCE
    5% BENZOYL PEROXIDE FOLLICULITIS CREAM 
    5% benzoyl peroxide folliculitis cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84558-026
    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
    CERAMIDE NP (UNII: 4370DF050B)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    AQUA (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERYL STEARATE (UNII: 230OU9XXE4)  
    CETEARYL ALCOHOL (UNII: 2DMT128M1S)  
    SQUALANE (UNII: GW89575KF9)  
    ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    DEXPANTHENOL (UNII: 1O6C93RI7Z)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ALLANTOIN (UNII: 344S277G0Z)  
    SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)  
    MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)  
    MAGNESIUM ALUMINOMETASILICATE (UNII: 9T3UU8T0QK)  
    FORSYTHIA SUSPENSA FRUIT (UNII: P4793M1ES5)  
    PURSLANE (UNII: M6S840WXG5)  
    MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    MENTHYL LACTATE (UNII: 2BF9E65L7I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84558-026-01100 g in 1 BOTTLE; Type 0: Not a Combination Product07/17/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00507/17/2026
    Labeler - GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd (545488483)
    Establishment
    NameAddressID/FEIBusiness Operations
    GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd545488483manufacture(84558-026)