Label: DR. THROWERS BPO 5- benzoyl peroxide cream

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated May 22, 2015

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  • DIRECTIONS:

    APPLY MEDICATION TO OILY AREAS OF THE FACE AND SHAVING BUMPS IN A VERY THIN LAYER. LEAVE ON OVERNIGHT. FREQUENCY OF APPLICATION: DETERMINED BY DR. THROWER.

  • USES:

    ACNE AND SHAVING BUMPS.

  • INGREDIENTS:

    Aqua, Ceteraryl Alcohol, Sodium Cetearyl Sulfate, Caprylic/Capric Triglyceride,Cyclopentasiloxane, Cyclohexasiloxane, Propylene Glycol, Decyl Oleate, Hydrogenated Elaesis Guineensis (Palm Kernal) Oil, Hydrogenated Glycine Soja (Soybean) Oil, Hydrogenated Gossypium Herbaceum (Cotton) Seed Oil, Lecithin, Diazolidinyl Urea, Methylparaben, Propylparaben, MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL, BISABOLOL, Tocopheryl Acetate, Disodium EDTA, Sodium Hyaluronate, Citric Acid, Aloe Barbadensis (Aloe) Leaf Juice

  • WARNINGS

    STOP IF SKIN BECOMES IRRITATED (PINK, RED DARKER, OR EXCESSIVE PEELING). COTACT DR. THROWER FOR INSTRUCTIONS. FOR EXTERNAL USE ONLY. KEEP OUT OF REACH OF CHILDREN. FEDERAL LAW PROHIBITS THE TRANSFER OF THIS DRUG TO ANY OTHER PERSON OTHER THAN FOR WHOM IT IS PRESCRIBED.

  • PRINCIPAL DISPLAY PANEL

    BPO-5 Label

  • INGREDIENTS AND APPEARANCE
    DR. THROWERS BPO 5 
    benzoyl peroxide cream
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:69299-103
    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)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DECYL OLEATE (UNII: ZGR06DO97T)  
    HYDROGENATED PALM KERNEL OIL (UNII: FM8D1RE2VP)  
    HYDROGENATED SOYBEAN OIL (UNII: A2M91M918C)  
    HYDROGENATED COTTONSEED OIL (UNII: Z82Y2C65EA)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69299-103-2256 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/15/2015
    Labeler - DR. THROWER'S SKINCARE, INC. (078711495)
    Registrant - DR. THROWER'S SKINCARE, INC. (078711495)