Label: DR. THROWERS BETA- 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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  • USES

    ECZEMA, SPECIFIC DRY SKIN, AND SPECIFIC SKIN IRRITATIONS.

  • DIRECTIONS:

    APPLY MEDICATION TO AREA OF SKIN IRRITATION IN A VERY THIN LAYER. LEAVE ON OVERNIGHT.

    FREQUENCY OF APPLICATION: DETERMINED BY DR. THROWER.

  • INGREDIENTS:

    AQUA, CETEARYL ALCOHOL, SODIUM CETEARYL SULFATE, CAPRYLIC/CAPRIC TRIGLYCERIDES, CYCLOPENTASILOXANE, CYCLOHEXASILOXANE, PROPYLENE GLYCOL, ALCOHOL DENATURED, DECYL OLEATE, HYDROGENATED ELAESIS GUINEENSIS (PALM KERNEL) OIL, HYDROGENATED GLYCINE SOYA (SOYBEAN) OIL, HYDROGENATED GOSSYPIUM HERBACEUM (COTTON) SEED OIL, LECITHIN, DIAZOLYDINYL UREA, METHYLPARABEN, PROPYLPARABEN, 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). CONTACT 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 PRESCRIBED.

  • PRINCIPAL DISPLAY PANEL

    Beta-Cream Label

  • INGREDIENTS AND APPEARANCE
    DR. THROWERS BETA 
    betamethasone dipropionate cream
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:69299-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETAMETHASONE DIPROPIONATE (UNII: 826Y60901U) (BETAMETHASONE - UNII:9842X06Q6M) BETAMETHASONE0.05 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)  
    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)  
    .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:69299-201-2256 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)
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