HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025%
HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025%
Approved
Approval ID
891b8160-c5db-91fd-e053-2a95a90a818b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 17, 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 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025%
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72934-6102
Product Classification
G
Generic Name
HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025%
Product Specifications
Route of AdministrationTOPICAL
Effective DateMay 17, 2019
FDA Product Classification
INGREDIENTS (3)
HYDROCORTISONEActive
Quantity: 0.5 g in 100 g
Code: WI4X0X7BPJ
Classification: ACTIB
HYDROQUINONEActive
Quantity: 4 g in 100 g
Code: XV74C1N1AE
Classification: ACTIB
TRETINOINActive
Quantity: 0.025 g in 100 g
Code: 5688UTC01R
Classification: ACTIB