"82442-694-04" National Drug Code (NDC)

NDC Code	82442-694-04
Package Description	1 BOTTLE in 1 CARTON (82442-694-04) / 118 mL in 1 BOTTLE
Product NDC	82442-694
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Up And Up Daytime Childrens Multi Symptom Cold
Non-Proprietary Name	Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	20240719
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M012
Manufacturer	Target Corporation
Substance Name	DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength	5; 100; 2.5
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]