Label: DR. THROWERS PBC NO. 1- hydroquinone, tretinoin, betamethasone dipropionate cream

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

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Drug Label Information

Updated May 22, 2015

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  • DIRECTIONS:

    APPLY IN A VERY THIN LAYER IN THE DARK AREA ONLY. FOR DARK SPOTS APPLY TO THE CENTER OF DARK SPOTS.

    FREQUENCY OF APPLICATION: DETERMINED BY DR. THROWER.

  • USES:

    EXTREME SKIN DISCOLORATION AND DARK SPOTS.

  • INGREDIENTS:

    Aqua, Ceteraryl Alcohol, Sodium Cetearyl Sulfate, Caprylic/Capric Triglyceride,Cyclopentasiloxane, Cyclohexasiloxane, Propylene Glycol, Butylene Glycol , Hydrogenated Lecithin,Sodium Oleate , Oligopeptide-68, Propanediol, Boerhavia Diffusa Root Extract ,Alcohol Denatured, Decyl Oleate, Hydrogenated Elaesis Guineensis (Palm Kernal) Oil, Hydrogenated Glycine Soja (Soybean) Oil, Hydrogenated Gossypium Herbaceum (Cotton) Seed Oil, Lecithin, Diazolidinyl Urea , Methylparaben, Propylparaben,Sodium Metabisulfite, Tocopheryl Acetate, Disodium EDTA, Sodium Hyaluronate, , Citric Acid , Aloe Barbadensis (Aloe) Leaf Juice

  • WARNINGS

    STOP USE IF SKIN BECOMES IRRITATED (PINK, RED DARKER, OR EXCESSIVE PEELING). 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

    PBC-1 Label

  • INGREDIENTS AND APPEARANCE
    DR. THROWERS PBC NO. 1 
    hydroquinone, tretinoin, betamethasone dipropionate cream
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:69299-301
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE12 g  in 100 g
    TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN0.1 g  in 100 g
    BETAMETHASONE DIPROPIONATE (UNII: 826Y60901U) (BETAMETHASONE - UNII:9842X06Q6M) BETAMETHASONE0.5 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)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
    SODIUM OLEATE (UNII: 399SL044HN)  
    AMINO ACIDS (UNII: 0O72R8RF8A)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    BOERHAVIA DIFFUSA ROOT (UNII: KR0SR09KYL)  
    ALCOHOL (UNII: 3K9958V90M)  
    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)  
    SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
    .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:69299-301-2128 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)
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