"71141-136-32" National Drug Code (NDC)

NDC Code	71141-136-32
Package Description	1 BOTTLE, PLASTIC in 1 BOX (71141-136-32) / 30 TABLET in 1 BOTTLE, PLASTIC
Product NDC	71141-136
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Mucus Relief
Proprietary Name Suffix	Dm
Non-Proprietary Name	Guaifenesin, Dextromethorphan Hbr
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20170228
End Marketing Date	20250228
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M012
Manufacturer	Lidl US, LLC
Substance Name	DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength	20; 400
Strength Unit	mg/1; mg/1
Pharmacy Classes	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]