141016 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025%
141016 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025%
Approved
Approval ID
a97c74e8-0132-1209-e053-2995a90a8592
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 2, 2020
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.
141016 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025%
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72934-6225
Product Classification
G
Generic Name
141016 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025%
Product Specifications
Route of AdministrationTOPICAL
Effective DateJuly 2, 2020
FDA Product Classification
INGREDIENTS (3)
HYDROQUINONEActive
Quantity: 4 g in 100 g
Code: XV74C1N1AE
Classification: ACTIB
HYDROCORTISONEActive
Quantity: 0.5 g in 100 g
Code: WI4X0X7BPJ
Classification: ACTIB
TRETINOINActive
Quantity: 0.025 g in 100 g
Code: 5688UTC01R
Classification: ACTIB