Desonide
DESONIDE OINTMENT, 0.05%
Approved
Approval ID
10feb882-10f0-4e5a-8481-bcaac54dfd52
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 19, 2011
Manufacturers
FDA
Physicians Total Care, Inc.
DUNS: 194123980
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Desonide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-4453
Application NumberNDA017426
Product Classification
M
Marketing Category
C73594
G
Generic Name
Desonide
Product Specifications
Route of AdministrationTOPICAL
Effective DateDecember 19, 2011
FDA Product Classification
INGREDIENTS (2)
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT
DESONIDEActive
Quantity: 0.5 mg in 1 g
Code: J280872D1O
Classification: ACTIB