| NDC Code | 50804-316-08 | 
|---|
			| Package Description | 245 mL in 1 BOTTLE, PLASTIC (50804-316-08) | 
|---|
			| Product NDC | 50804-316 | 
|---|
			| Product Type Name | HUMAN OTC DRUG | 
|---|
			| Proprietary Name | Severe Cold And Cough Relief | 
|---|
			| Proprietary Name Suffix | Daytime | 
|---|
			| Non-Proprietary Name | Acetaminohpen, Dextromethorphan Hbr, Phenylephrine Hcl | 
|---|
			| Dosage Form | LIQUID | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20160731 | 
|---|
			| End Marketing Date | 20250731 | 
|---|
			| Marketing Category Name | OTC MONOGRAPH FINAL | 
|---|
			| Application Number | part341 | 
|---|
			| Manufacturer | Good Sense (Geiss, Destin & Dunn, Inc.) | 
|---|
			| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE | 
|---|
			| Strength | 650; 20; 10 | 
|---|
			| Strength Unit | mg/30mL; mg/30mL; mg/30mL | 
|---|
			| 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] | 
|---|