NDC Code | 72934-1126-2 |
Package Description | 30 g in 1 BOTTLE, PUMP (72934-1126-2) |
Product NDC | 72934-1126 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Imiquimod 5% / Levocetirizine Dihydrochloride 1% / Tretinoin 0.05% |
Non-Proprietary Name | Imiquimod 5% / Levocetirizine Dihydrochloride 1% / Tretinoin 0.05% |
Dosage Form | GEL |
Usage | TOPICAL |
Start Marketing Date | 20190501 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Manufacturer | Sincerus Florida, LLC |
Substance Name | TRETINOIN; LEVOCETIRIZINE DIHYDROCHLORIDE; IMIQUIMOD |
Strength | .05; 1; 5 |
Strength Unit | g/100g; g/100g; g/100g |
Pharmacy Classes | Retinoid [EPC],Retinoids [CS],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC],Increased Cytokine Activity [PE],Increased Cytokine Production [PE],Interferon Inducers [MoA] |