MINOXIDIL 7% / PROGESTERONE 0.1% / TRETINOIN 0.025%
MINOXIDIL 7% / PROGESTERONE 0.1% / TRETINOIN 0.025%
Approved
Approval ID
883a3678-fea4-2d24-e053-2995a90a0666
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.
MINOXIDIL 7% / PROGESTERONE 0.1% / TRETINOIN 0.025%
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72934-4149
Product Classification
G
Generic Name
MINOXIDIL 7% / PROGESTERONE 0.1% / TRETINOIN 0.025%
Product Specifications
Route of AdministrationTOPICAL
Effective DateMay 6, 2019
FDA Product Classification
INGREDIENTS (3)
PROGESTERONEActive
Quantity: 0.1 g in 100 g
Code: 4G7DS2Q64Y
Classification: ACTIB
MINOXIDILActive
Quantity: 7 g in 100 g
Code: 5965120SH1
Classification: ACTIB
TRETINOINActive
Quantity: 0.025 g in 100 g
Code: 5688UTC01R
Classification: ACTIB