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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72934-5069
Product Classification
G
Generic Name
DESOXIMETASONE 0.05% / NIACINAMIDE 4%
Product Specifications
Route of AdministrationTOPICAL
Effective DateMay 22, 2019
FDA Product Classification
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