Desoximetasone
Desoximetasone Gel USP, 0.05%For topical use only. Not for oral, ophthalmic or intravaginal use.Rx Only
Approved
Approval ID
ede7f6fa-d128-4058-a7c4-d212798f8b01
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 12, 2016
Manufacturers
FDA
GROUPE PARIMA INC
DUNS: 252437850
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Desoximetasone
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code65179-501
Application NumberANDA204675
Product Classification
M
Marketing Category
C73584
G
Generic Name
Desoximetasone
Product Specifications
Route of AdministrationTOPICAL
Effective DateAugust 25, 2016
FDA Product Classification
INGREDIENTS (8)
DESOXIMETASONEActive
Quantity: 0.5 mg in 1 g
Code: 4E07GXB7AU
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
DOCUSATE SODIUMInactive
Code: F05Q2T2JA0
Classification: IACT
EDETATE DISODIUMInactive
Code: 7FLD91C86K
Classification: IACT
ISOPROPYL MYRISTATEInactive
Code: 0RE8K4LNJS
Classification: IACT
CARBOMER HOMOPOLYMER TYPE CInactive
Code: 4Q93RCW27E
Classification: IACT
ALCOHOLInactive
Code: 3K9958V90M
Classification: IACT
TROLAMINEInactive
Code: 9O3K93S3TK
Classification: IACT