Desonide
Desonide Cream, 0.05%
Approved
Approval ID
c70aabe7-c044-40cd-b17d-35c665160c9c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 3, 2023
Manufacturers
FDA
Bryant Ranch Prepack
DUNS: 171714327
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Desonide
PRODUCT DETAILS
NDC Product Code63629-2506
Application NumberANDA210198
Marketing CategoryC73584
Route of AdministrationTOPICAL
Effective DateMay 19, 2021
Generic NameDesonide
INGREDIENTS (12)
DESONIDEActive
Quantity: 0.5 mg in 1 g
Code: J280872D1O
Classification: ACTIB
ALUMINUM SULFATEInactive
Code: 34S289N54E
Classification: IACT
CETOSTEARYL ALCOHOLInactive
Code: 2DMT128M1S
Classification: IACT
CALCIUM ACETATEInactive
Code: Y882YXF34X
Classification: IACT
LIGHT MINERAL OILInactive
Code: N6K5787QVP
Classification: IACT
ICODEXTRINInactive
Code: 2NX48Z0A9G
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
METHYLPARABENInactive
Code: A2I8C7HI9T
Classification: IACT
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT
YELLOW WAXInactive
Code: 2ZA36H0S2V
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT