| NDC Code | 55959-132-01 | 
|---|
			| Package Description | 1 BLISTER PACK in 1 BOX (55959-132-01)  > 12 TABLET in 1 BLISTER PACK | 
|---|
			| Product NDC | 55959-132 | 
|---|
			| Product Type Name | HUMAN OTC DRUG | 
|---|
			| Proprietary Name | Dolomax Cold Cough | 
|---|
			
			| Non-Proprietary Name | Acetaminophen, Guaifenesin, Phenylephrine Hcl, Dextromethorphan | 
|---|
			| Dosage Form | TABLET | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20171201 | 
|---|
			| End Marketing Date | 20221031 | 
|---|
			| Marketing Category Name | OTC MONOGRAPH FINAL | 
|---|
			| Application Number | part341 | 
|---|
			| Manufacturer | BENARD INDUSTRIES INC | 
|---|
			| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE | 
|---|
			| Strength | 325; 15; 200; 5 | 
|---|
			| Strength Unit | mg/1; mg/1; mg/1; mg/1 | 
|---|
			| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC] | 
|---|