Label: DR. THROWERS PBC NO. 1- hydroquinone, tretinoin, betamethasone dipropionate cream
-
Contains inactivated NDC Code(s)
NDC Code(s): 69299-301-21 - Packager: DR. THROWER'S SKINCARE, INC.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated May 22, 2015
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DIRECTIONS:
- USES:
-
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
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DR. THROWERS PBC NO. 1
hydroquinone, tretinoin, betamethasone dipropionate creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69299-301 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE 12 g in 100 g TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN 0.1 g in 100 g BETAMETHASONE DIPROPIONATE (UNII: 826Y60901U) (BETAMETHASONE - UNII:9842X06Q6M) BETAMETHASONE 0.5 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) 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:69299-301-21 28 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)