Label: DR. THROWERS BETA- betamethasone dipropionate cream
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Contains inactivated NDC Code(s)
NDC Code(s): 69299-201-22 - 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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- USES
- DIRECTIONS:
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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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR. THROWERS BETA
betamethasone dipropionate creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69299-201 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETAMETHASONE DIPROPIONATE (UNII: 826Y60901U) (BETAMETHASONE - UNII:9842X06Q6M) BETAMETHASONE 0.05 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:69299-201-22 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)