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Desoximetasone

Desoximetasone Cream USP, 0.05%, Cream USP, 0.25%Gel USP, 0.05%

Approved
Approval ID

c5febbe3-7d06-463e-ba36-879a71eba9df

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Oct 8, 2009

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.

Desoximetasone

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code54868-3041
Application NumberANDA073193
Product Classification
M
Marketing Category
C73584
G
Generic Name
Desoximetasone
Product Specifications
Route of AdministrationTOPICAL
Effective DateJanuary 12, 2011
FDA Product Classification

INGREDIENTS (6)

DESOXIMETASONEActive
Quantity: 2.5 mg in 1 g
Code: 4E07GXB7AU
Classification: ACTIB
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
ISOPROPYL MYRISTATEInactive
Code: 0RE8K4LNJS
Classification: IACT
MINERAL OILInactive
Code: T5L8T28FGP
Classification: IACT
CETOSTEARYL ALCOHOLInactive
Code: 2DMT128M1S
Classification: IACT

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Desoximetasone - FDA Drug Approval Details