NDC Code | 72934-4080-8 |
Package Description | 60 g in 1 BOTTLE, GLASS (72934-4080-8) |
Product NDC | 72934-4080 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Fluocinolone Acetonide 0.01% / Minoxidil 7% / Progesterone 0.1% |
Non-Proprietary Name | Fluocinolone Acetonide 0.01% / Minoxidil 7% / Progesterone 0.1% |
Dosage Form | SOLUTION |
Usage | TOPICAL |
Start Marketing Date | 20190509 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Manufacturer | Sincerus florida, LLC |
Substance Name | FLUOCINOLONE ACETONIDE; MINOXIDIL; PROGESTERONE |
Strength | .01; 7; .1 |
Strength Unit | g/100g; g/100g; g/100g |
Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC],Progesterone [CS],Progesterone [EPC] |