Home NDC 67091-342 Mucus Relief DM
Product NDC 67091-342
11-digit product format 670910342
Labeler code 67091
Product ID 67091-342_5d6beb4c-031a-4fce-8627-00205c2c1680
Type HUMAN OTC DRUG
Nonproprietary name Dextromethorphan HBr and Guaifenesin
Dosage form SOLUTION
Route ORAL
Labeler WINCO FOODS, LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-07-16
Substance DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength 20; 400 mg/20mL; mg/20mL
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 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
Brand name suffix Maximum Strength
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROMETHORPHAN HYDROBROMIDE 20 mg/20mL GUAIFENESIN 400 mg/20mL
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 1020138 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 67091-342-06 Mucus Relief DMMaximum Strength 180 mL in 1 BOTTLE SOLUTION 180 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67091-342 MUCUS RELIEF DM MAXIMUM STRENGTH (DEXTROMETHORPHAN HBR AND GUAIFENESIN) SOLUTION [WINCO FOODS, LLC] 7 Current NDC, Legacy NDC, 1 package rows 20241121_e6afa830-6ce2-4abc-b5c9-3f5f156444df.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 99 of 180 · 3,583 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 67091-342-06 67091034206 180 mL in 1 BOTTLE (67091-342-06) 180 ml 2019-07-16 0000-00-00 No No Current