DR. THROWERS BETA

DR. THROWERS BETA- betamethasone dipropionate cream
DR. THROWER’S SKINCARE, INC.

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.

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.

Beta-Cream Label
(click image for full-size original)

DR. THROWERS BETA
betamethasone dipropionate cream
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69299-201
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BETAMETHASONE DIPROPIONATE (BETAMETHASONE) BETAMETHASONE 0.05 g in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER
CETOSTEARYL ALCOHOL
SODIUM CETOSTEARYL SULFATE
MEDIUM-CHAIN TRIGLYCERIDES
CYCLOMETHICONE 5
CYCLOMETHICONE 6
PROPYLENE GLYCOL
ALCOHOL
DECYL OLEATE
HYDROGENATED PALM KERNEL OIL
HYDROGENATED SOYBEAN OIL
HYDROGENATED COTTONSEED OIL
LECITHIN, SOYBEAN
DIAZOLIDINYL UREA
METHYLPARABEN
PROPYLPARABEN
.ALPHA.-TOCOPHEROL ACETATE
EDETATE DISODIUM
HYALURONATE SODIUM
ANHYDROUS CITRIC ACID
ALOE VERA LEAF
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:69299-201-22 56 g in 1 JAR None
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)

Revised: 05/2015 DR. THROWER’S SKINCARE, INC.

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