| NDC Code | 72934-4070-8 |
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| Package Description | 60 g in 1 BOTTLE, GLASS (72934-4070-8) |
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| Product NDC | 72934-4070 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dexamethasone Sodium Phosphate 0.1% / Finasteride 0.1% / Minoxidil 5% / Tretinoin 0.025% |
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| Non-Proprietary Name | Dexamethasone Sodium Phosphate 0.1% / Finasteride 0.1% / Minoxidil 5% / Tretinoin 0.025% |
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| Dosage Form | SOLUTION |
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| Usage | TOPICAL |
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| Start Marketing Date | 20190509 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | Sincerus Florida |
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| Substance Name | DEXAMETHASONE SODIUM PHOSPHATE; FINASTERIDE; MINOXIDIL; TRETINOIN |
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| Strength | .1; .1; 5; .025 |
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| Strength Unit | g/100g; g/100g; g/100g; g/100g |
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| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA],Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC],Retinoid [EPC],Retinoids [CS] |
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