Home NDC 0363-0533 Mucus Relief DM
Product NDC 0363-0533
11-digit product format 003630533
Labeler code 0363
Product ID 0363-0533_4d721ae5-176b-419f-b29b-a6c138a656f7
Type HUMAN OTC DRUG
Nonproprietary name Dextromethorphan HBr, Guaifenesin
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Walgreen Company
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2005-12-31
Substance DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength 20; 400 mg/1; mg/1
Pharmacologic 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]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 23 matching rows.
View current auxiliary records. · View the auxiliary file history.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Mucus Relief DM
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROMETHORPHAN HYDROBROMIDE 20 mg/1 GUAIFENESIN 400 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9D2RTI9KYH Internal UNII lookup 495W7451VQ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1147685 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0363-0533-01 Mucus Relief DM 1 in 1 CARTON TABLET, FILM COATED 1 20 0363-0533-01 Mucus Relief DM 30 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 30 20 0363-0533-11 Mucus Relief DM 1 in 1 CARTON TABLET, FILM COATED 1 20 0363-0533-11 Mucus Relief DM 60 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 60 20 0363-0533-25 Mucus Relief DM 1 in 1 CARTON TABLET, FILM COATED 1 20 0363-0533-25 Mucus Relief DM 45 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 45 20 0363-0533-32 Mucus Relief DM 60 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 60 20 0363-0533-32 Mucus Relief DM 2 in 1 CARTON TABLET, FILM COATED 2 20
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0363-0533 MUCUS RELIEF DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) TABLET, FILM COATED [WALGREEN COMPANY] 19 Current NDC, Legacy NDC, 8 package rows 20250510_cad5da8c-65a6-44c4-a4c7-38f2c7fe43aa.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 73 of 178 · 3,550 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0363-0533-01 00363053301 1 BOTTLE, PLASTIC in 1 CARTON (0363-0533-01) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2005-12-31 0000-00-00 No No Current 0363-0533-11 00363053311 1 BOTTLE, PLASTIC in 1 CARTON (0363-0533-11) > 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2005-12-31 0000-00-00 No No Current 0363-0533-25 00363053325 1 BOTTLE in 1 CARTON (0363-0533-25) > 45 TABLET, FILM COATED in 1 BOTTLE 1 bottle 2005-12-31 0000-00-00 No No Current 0363-0533-32 00363053332 2 BOTTLE, PLASTIC in 1 CARTON (0363-0533-32) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2005-12-31 0000-00-00 No No Current