Home NDC 30142-508 Mucus Relief DM
Product NDC 30142-508
11-digit product format 301420508
Labeler code 30142
Product ID 30142-508_b2cdb67b-b9d5-4a34-b01b-dce6d813ede3
Type HUMAN OTC DRUG
Nonproprietary name Dextromethorphan Hydrobromide Guaifenesin
Dosage form LIQUID
Route ORAL
Labeler The Kroger Co.
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-09-01
Marketing end 2026-12-28
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
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 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 30142-508-06 Mucus Relief DM 177 mL in 1 BOTTLE, PLASTIC LIQUID 177 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 30142-508 MUCUS RELIEF DM (DEXTROMETHORPHAN HYDROBROMIDE GUAIFENESIN) LIQUID [THE KROGER CO.] 2 Current NDC, Legacy NDC, 1 package rows 20240612_49829083-5c0a-4620-bfb3-7103642368db.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 · 3,551 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 30142-508-06 30142050806 177 mL in 1 BOTTLE, PLASTIC (30142-508-06) 177 ml 2020-09-01 2026-12-28 No No Current