MedPath

DESOXIMETASONE 0.05% / NIACINAMIDE 4%

DESOXIMETASONE 0.05% / NIACINAMIDE 4%

Approved
Approval ID

89804cbd-4acd-9241-e053-2995a90a8a24

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

May 22, 2019

Manufacturers
FDA

Sincerus Florida, LLC

DUNS: 080105003

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

DESOXIMETASONE 0.05% / NIACINAMIDE 4%

PRODUCT DETAILS

NDC Product Code72934-5069
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationTOPICAL
Effective DateMay 22, 2019
Generic NameDESOXIMETASONE 0.05% / NIACINAMIDE 4%

INGREDIENTS (2)

NIACINAMIDEActive
Quantity: 4 g in 100 g
Code: 25X51I8RD4
Classification: ACTIB
DESOXIMETASONEActive
Quantity: 0.05 g in 100 g
Code: 4E07GXB7AU
Classification: ACTIB
© Copyright 2025. All Rights Reserved by MedPath
DESOXIMETASONE 0.05% / NIACINAMIDE 4% - FDA Approval | MedPath