| NDC Code | 63868-235-06 |
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| Package Description | 177 mL in 1 BOTTLE, PLASTIC (63868-235-06) |
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| Product NDC | 63868-235 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Mucus Relief Dm Max |
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| Proprietary Name Suffix | Maximum Strength |
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| Non-Proprietary Name | Dextromethorphan Hbr, Guaifenesin |
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| Dosage Form | LIQUID |
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| Usage | ORAL |
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| Start Marketing Date | 20160331 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M012 |
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| Manufacturer | QUALITY CHOICE (Chain Drug Marketing Association) |
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| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
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| Strength | 20; 400 |
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| Strength Unit | mg/20mL; mg/20mL |
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| Pharmacy Classes | Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA] |
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