Label: DR. THROWERS HYDROTET- tretinoin, hydrocortisone 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 MEDICATION TO OILY AREA ONLY OF THE FACE IN VERY THIN LAYER. LEAVE ON OVERNIGHT.

  • PURPOSE:

    RX STRENGTH TOPICAL RETINOID FOR TREATMENT OF ACNE, SHAVING BUMPS, AND SPECIFIC BUMPY SKIN PROBLEMS. LEAVES SKIN SMOOTH, CLEAR AND NEW.

    uSES: ACNE AND SPECIFIC SKIN CONDITIONS.

  • INGREDIENTS:

    Aqua, Ceteraryl Alcohol, Sodium Cetearyl Sulfate, Caprylic/Capric Triglyceride,Cyclopentasiloxane, Cyclohexasiloxane, Propylene Glycol, 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, 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 IT IS PRESCRIBED.

  • PRINCIPAL DISPLAY PANEL

    Hydrotet Cream Label

  • INGREDIENTS AND APPEARANCE
    DR. THROWERS HYDROTET 
    tretinoin, hydrocortisone cream
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:69299-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN0.05 g  in 100 g
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE1 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:69299-102-2256 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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