Home NDC 72854-209 Mucinex Nightshift Sinus
Product NDC 72854-209
11-digit product format 728540209
Labeler code 72854
Product ID 72854-209_35322ca5-3819-1ec8-e063-6394a90a262f
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Dextromethorphan Hydrobromide, and Triprolidine Hydrochloride
Dosage form TABLET, COATED
Route ORAL
Labeler RB Health (US) LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-01
Substance DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; TRIPROLIDINE HYDROCHLORIDE
Active strength 10; 325; 1.25 mg/1; 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 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 Mucinex Nightshift Sinus
Brand name suffix Maximum Strength
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROMETHORPHAN HYDROBROMIDE 10 mg/1 ACETAMINOPHEN 325 mg/1 TRIPROLIDINE HYDROCHLORIDE 1.25 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9D2RTI9KYH Internal UNII lookup 362O9ITL9D Internal UNII lookup YAN7R5L890 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2549034 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 72854-209-20 Mucinex Nightshift SinusMaximum Strength 10 in 1 BLISTER PACK TABLET, COATED 10 2 72854-209-20 Mucinex Nightshift SinusMaximum Strength 2 in 1 CARTON TABLET, COATED 2 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72854-209 MUCINEX NIGHTSHIFT SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND TRIPROLIDINE HYDROCHLORIDE) TABLET, COATED [RB HEALTH (US) LLC] 2 Current NDC, 2 package rows 20250519_35322238-d498-1a52-e063-6394a90ac9c4.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 Sample Exclude flag Status 72854-209-20 72854020920 2 BLISTER PACK in 1 CARTON (72854-209-20) / 10 TABLET, COATED in 1 BLISTER PACK 2 blister pack 2025-05-01 No No Current