HYDROCORTISONE 2.5% / IODOQUINOL 1% / KETOCONAZOLE 2%
HYDROCORTISONE 2.5% / IODOQUINOL 1% / KETOCONAZOLE 2%
Approved
Approval ID
8902658c-b01c-1761-e053-2a95a90a1f80
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 16, 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.
HYDROCORTISONE 2.5% / IODOQUINOL 1% / KETOCONAZOLE 2%
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72934-2111
Product Classification
G
Generic Name
HYDROCORTISONE 2.5% / IODOQUINOL 1% / KETOCONAZOLE 2%
Product Specifications
Route of AdministrationTOPICAL
Effective DateMay 16, 2019
FDA Product Classification
INGREDIENTS (3)
HYDROCORTISONEActive
Quantity: 2.5 g in 100 g
Code: WI4X0X7BPJ
Classification: ACTIB
IODOQUINOLActive
Quantity: 1 g in 100 g
Code: 63W7IE88K8
Classification: ACTIB
KETOCONAZOLEActive
Quantity: 2 g in 100 g
Code: R9400W927I
Classification: ACTIB