Label: DR. THROWERS HYDROTET- tretinoin, hydrocortisone cream
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Contains inactivated NDC Code(s)
NDC Code(s): 69299-102-22 - Packager: DR. THROWER'S SKINCARE, INC.
- 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:
- PURPOSE:
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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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR. THROWERS HYDROTET
tretinoin, hydrocortisone creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69299-102 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN 0.05 g in 100 g HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 1 g in 100 g Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:69299-102-22 56 g in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/15/2015 Labeler - DR. THROWER'S SKINCARE, INC. (078711495) Registrant - DR. THROWER'S SKINCARE, INC. (078711495)