Home NDC 17714-150-60 Mucus Relief Cough and Congestion DM
Product NDC 17714-150
Requested package NDC 17714-150-60
11-digit product format 177140150
Labeler code 17714
Product ID 17714-150_5cc973b8-e550-2f6c-e053-2a91aa0a9ab8
Type HUMAN OTC DRUG
Nonproprietary name Guaifenesin and Dextromethorphan HBr
Dosage form TABLET
Route ORAL
Labeler Advance Pharmaceutical Inc.
Application part341
Marketing category OTC MONOGRAPH FINAL
Marketing start 2017-08-01
Substance DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength 20; 400 mg/1; mg/1
Pharmacologic classes 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 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Mucus Relief Cough and Congestion DM
Listing expiration 2026-12-31 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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 17714-150-60 Mucus Relief Cough and Congestion DM 60 in 1 BOTTLE TABLET 60 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 17714-150 MUCUS RELIEF COUGH AND CONGESTION DM (GUAIFENESIN AND DEXTROMETHORPHAN HBR) TABLET [ADVANCE PHARMACEUTICAL INC.] 2 Current NDC, Legacy NDC, 1 package rows 20171031_e507a84a-59d5-47f2-a2df-f342e4b093b4.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 1 of 1 · 1 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 17714-150-60 17714015060 60 TABLET in 1 BOTTLE (17714-150-60) 60 tablet 2017-08-01 0000-00-00 No No Current