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NDC 00363-0474-01 Mucus Relief DM 30; 600 mg/1; mg/1 Details

Mucus Relief DM 30; 600 mg/1; mg/1

Mucus Relief DM is a ORAL TABLET, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by WALGREEN CO.. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN.

MedlinePlus Drug Summary

Dextromethorphan is used to temporarily relieve cough caused by the common cold, the flu, or other conditions. Dextromethorphan will relieve a cough but will not treat the cause of the cough or speed recovery. Dextromethorphan is in a class of medications called antitussives. It works by decreasing activity in the part of the brain that causes coughing.

Related Packages: 00363-0474-01
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Dextromethorphan

Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a class of medications called expectorants. It works by thinning the mucus in the air passages to make it easier to cough up the mucus and clear the airways.

Related Packages: 00363-0474-01
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Guaifenesin

Product Information

NDC	00363-0474
Product ID	0363-0474_ba30d7fd-2984-4e14-b2d3-f3a6e04f98ff
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Mucus Relief DM
Proprietary Name Suffix	n/a
Non-Proprietary Name	Guaifenesin and Dextromethorphan HBr
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	30; 600
Active Ingredient Units	mg/1; mg/1
Substance Name	DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Labeler Name	WALGREEN CO.
Pharmaceutical Class	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 Ant
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA206941
Listing Certified Through	2024-12-31

Package

NDC 00363-0474-01 (00363047401)

Pricing Information	N/A
NDC Package Code	0363-0474-01
Billing NDC	00363047401
Package	4 BLISTER PACK in 1 CARTON (0363-0474-01) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Marketing Start Date	2017-03-17
NDC Exclude Flag	N