"0031-8742-20" National Drug Code (NDC)

NDC Code	0031-8742-20
Package Description	1 BOTTLE in 1 CARTON (0031-8742-20) / 237 mL in 1 BOTTLE
Product NDC	0031-8742
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Robitussin Peak Cold Multi-symptom Cold
Non-Proprietary Name	Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20110612
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M012
Manufacturer	Haleon US Holdings LLC
Substance Name	DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength	10; 100; 5
Strength Unit	mg/5mL; mg/5mL; mg/5mL
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]