Home NDC 41250-776 Maximum Strength Mucus Relief Severe Congestion and Cough
Product NDC 41250-776
11-digit product format 412500776
Labeler code 41250
Product ID 41250-776_0232ff89-461a-4a26-969a-28132bca83b8
Type HUMAN OTC DRUG
Nonproprietary name dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Dosage form LIQUID
Route ORAL
Labeler MEIJER DISTRIBUTION INC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-03-14
Substance DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Active strength 20; 400; 10 mg/20mL; mg/20mL; mg/20mL
Pharmacologic classes Adrenergic alpha1-Agonists [MoA], 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], alpha-1 Adrenergic Agonist [EPC]
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 Maximum Strength Mucus Relief Severe Congestion and Cough
Brand name suffix Cooling Menthol
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROMETHORPHAN HYDROBROMIDE 20 mg/20mL GUAIFENESIN 400 mg/20mL PHENYLEPHRINE HYDROCHLORIDE 10 mg/20mL
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 41250-776-06 Maximum Strength Mucus Relief Severe Congestion and CoughCooling Menthol 180 mL in 1 BOTTLE, PLASTIC LIQUID 180 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-776 MAXIMUM STRENGTH MUCUS RELIEF SEVERE CONGESTION AND COUGH COOLING MENTHOL (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE) LIQUID [MEIJER DISTRIBUTION INC] 7 Current NDC, Legacy NDC, 1 package rows 20241023_ab8322f6-8474-4043-8f2b-a71e3f3b48ce.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 74 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 41250-776-06 41250077606 180 mL in 1 BOTTLE, PLASTIC (41250-776-06) 180 ml 2017-03-14 0000-00-00 No No Current