Betamethasone Ointment Augmented
Name: Betamethasone Ointment Augmented
Indications and Usage for Betamethasone Ointment Augmented
Betamethasone dipropionate ointment (augmented), 0.05% is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients 13 years of age or older.
Betamethasone Ointment Augmented Description
Betamethasone Dipropionate Ointment USP (Augmented), 0.05% contains betamethasone dipropionate USP, a synthetic adrenocorticosteroid, for topical use. Betamethasone, an analog of prednisolone, has a high degree of corticosteroid activity and a slight degree of mineralocorticoid activity. Betamethasone dipropionate is the 17,21-dipropionate ester of betamethasone.
Chemically, betamethasone dipropionate is 9-fluoro-11β,17,21-trihydroxy-16β-methylpregna-1,4-diene-3,20-dione 17,21-dipropionate, with the molecular formula C28H37FO7, a molecular weight of 504.6 and the following structural formula:
Betamethasone dipropionate is a white to creamy-white, odorless powder insoluble in water; freely soluble in acetone and in chloroform; sparingly soluble in alcohol.
Each gram of Betamethasone Dipropionate Ointment USP (Augmented), 0.05% contains: 0.643 mg betamethasone dipropionate, USP (equivalent to 0.5 mg betamethasone) in a white to off-white ointment base of propylene glycol, propylene glycol monostearate, beeswax and white petrolatum.
PRINCIPAL DISPLAY PANEL - 15 g Tube
NDC 0168-0268-15
Fougera®
BETAMETHASONEDIPROPIONATE OINTMENT
USP (AUGMENTED), 0.05%*
*Strength expressed as betamethasone
Rx only
For topical use only.Not for oral, ophthalmic, or
intravaginal use.
NET WT 15 grams