"69842-723-62" National Drug Code (NDC)

NDC Code	69842-723-62
Package Description	12 BLISTER PACK in 1 CARTON (69842-723-62) / 2 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC	69842-723
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Cooling Severe Daytime
Non-Proprietary Name	Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20200207
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M012
Manufacturer	CVS Pharmacy
Substance Name	ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength	325; 10; 200; 5
Strength Unit	mg/1; mg/1; mg/1; mg/1
Pharmacy Classes	Adrenergic alpha1-Agonists [MoA], 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], alpha-1 Adrenergic Agonist [EPC]