| NDC Code | 70677-0139-2 |
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| Package Description | 1 BOTTLE in 1 CARTON (70677-0139-2) / 236 mL in 1 BOTTLE |
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| Product NDC | 70677-0139 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Sunmark Adult Tussin Dm |
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| Non-Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20220427 |
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| End Marketing Date | 20250930 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M012 |
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| Manufacturer | Strategic Sourcing Services LLC |
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| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
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| Strength | 20; 200 |
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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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