DESOXIMETASONE 0.05% / HYDROQUINONE 6% / TRETINOIN 0.05%
DESOXIMETASONE 0.05% / HYDROQUINONE 6% / TRETINOIN 0.05%
Approved
Approval ID
89585e3f-167e-dd3b-e053-2995a90ade55
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 20, 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% / HYDROQUINONE 6% / TRETINOIN 0.05%
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72934-6067
Product Classification
G
Generic Name
DESOXIMETASONE 0.05% / HYDROQUINONE 6% / TRETINOIN 0.05%
Product Specifications
Route of AdministrationTOPICAL
Effective DateMay 20, 2019
FDA Product Classification
INGREDIENTS (3)
DESOXIMETASONEActive
Quantity: 0.05 g in 100 g
Code: 4E07GXB7AU
Classification: ACTIB
HYDROQUINONEActive
Quantity: 6 g in 100 g
Code: XV74C1N1AE
Classification: ACTIB
TRETINOINActive
Quantity: 0.05 g in 100 g
Code: 5688UTC01R
Classification: ACTIB