hims hair regrowth treatment
HIMS Hair Regrowth Treatment Drug Facts
Approved
Approval ID
311a6712-092f-1eeb-e063-6394a90afcd1
Product Type
HUMAN OTC DRUG LABEL
Effective Date
Jan 1, 2023
Manufacturers
FDA
Praxis, LLC
DUNS: 016329513
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
minoxidil
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code59368-334
Application NumberANDA075598
Product Classification
M
Marketing Category
C73584
G
Generic Name
minoxidil
Product Specifications
Route of AdministrationTOPICAL
Effective DateJanuary 1, 2023
FDA Product Classification
INGREDIENTS (4)
ALCOHOLInactive
Code: 3K9958V90M
Classification: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
MINOXIDILActive
Quantity: 5 g in 100 mL
Code: 5965120SH1
Classification: ACTIB