| NDC Code | 72934-1129-2 |
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| Package Description | 30 g in 1 BOTTLE, PUMP (72934-1129-2) |
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| Product NDC | 72934-1129 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Imiquimod 5% / Tretinoin 0.025% |
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| Non-Proprietary Name | Imiquimod 5% / Tretinoin 0.025% |
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| Dosage Form | GEL |
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| Usage | TOPICAL |
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| Start Marketing Date | 20190507 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | Sincerus Florida, LLC |
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| Substance Name | TRETINOIN; IMIQUIMOD |
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| Strength | .025; 5 |
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| Strength Unit | g/100g; g/100g |
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| Pharmacy Classes | Retinoid [EPC],Retinoids [CS],Increased Cytokine Activity [PE],Increased Cytokine Production [PE],Interferon Inducers [MoA] |
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