| NDC Code | 63868-753-50 | 
|---|
			| Package Description | 1 BOTTLE in 1 CARTON (63868-753-50)  / 50 TABLET in 1 BOTTLE | 
|---|
			| Product NDC | 63868-753 | 
|---|
			| Product Type Name | HUMAN OTC DRUG | 
|---|
			| Proprietary Name | Quality Choice Mucus Relief Dm | 
|---|
			| Proprietary Name Suffix | Dm | 
|---|
			| Non-Proprietary Name | Dextromethorphan Hydrobromide / Guaifenesin | 
|---|
			| Dosage Form | TABLET | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20120801 | 
|---|
			
			| Marketing Category Name | OTC MONOGRAPH DRUG | 
|---|
			| Application Number | M012 | 
|---|
			| Manufacturer | Chain Drug Marketing Association | 
|---|
			| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN | 
|---|
			| Strength | 20; 400 | 
|---|
			| Strength Unit | mg/1; mg/1 | 
|---|
			| 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] | 
|---|