DR. THROWERS BETA- betamethasone dipropionate cream

DR. THROWERS BETA by

Drug Labeling and Warnings

DR. THROWERS BETA by is a Prescription medication manufactured, distributed, or labeled by DR. THROWER'S SKINCARE, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

DR. THROWERS BETA 
betamethasone dipropionate cream

Product 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)