IMIQUIMOD 5% / TRETINOIN 0.025%
IMIQUIMOD 5% / TRETINOIN 0.025%
Approved
Approval ID
8839ed49-b52a-11f6-e053-2a95a90a7492
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 6, 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.
IMIQUIMOD 5% / TRETINOIN 0.025%
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72934-1129
Product Classification
G
Generic Name
IMIQUIMOD 5% / TRETINOIN 0.025%
Product Specifications
Route of AdministrationTOPICAL
Effective DateMay 6, 2019
FDA Product Classification
INGREDIENTS (2)
TRETINOINActive
Quantity: 0.025 g in 100 g
Code: 5688UTC01R
Classification: ACTIB
IMIQUIMODActive
Quantity: 5 g in 100 g
Code: P1QW714R7M
Classification: ACTIB