Home NDC 49035-774 Maximum Strength Mucus Relief Severe Congestion and Cough
Product NDC 49035-774
11-digit product format 490350774
Labeler code 49035
Product ID 49035-774_44f50c26-25a8-5b34-e063-6294a90a6fbe
Type HUMAN OTC DRUG
Nonproprietary name dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Dosage form LIQUID
Route ORAL
Labeler Wal-Mart Stores,Inc.,
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-05-01
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 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 Maximum Strength Mucus Relief Severe Congestion and Cough
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROMETHORPHAN HYDROBROMIDE 20 mg/20mL GUAIFENESIN 400 mg/20mL PHENYLEPHRINE HYDROCHLORIDE 10 mg/20mL
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 495W7451VQ Internal UNII lookup 04JA59TNSJ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1043543 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 49035-774-06 Maximum Strength Mucus Relief Severe Congestion and Cough 180 mL in 1 BOTTLE, PLASTIC LIQUID 180 8 49035-774-09 Maximum Strength Mucus Relief Severe Congestion and Cough 266 mL in 1 BOTTLE, PLASTIC LIQUID 266 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49035-774 MAXIMUM STRENGTH MUCUS RELIEF SEVERE CONGESTION AND COUGH (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE) LIQUID [WAL-MART STORES,INC.,] 7 Current NDC, Legacy NDC, 1 package rows 20241116_770c0e4f-0eed-4b8c-85a5-761b6a84db62.zip 49035-774 MAXIMUM STRENGTH MUCUS RELIEF SEVERE CONGESTION AND COUGH (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE) LIQUID [WAL-MART STORES,INC.,] 7 Current NDC, Legacy NDC, 1 package rows 20241116_9c8c1974-f931-4493-abb5-ecdc32764ab3.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 49035-774-06 49035077406 180 mL in 1 BOTTLE, PLASTIC (49035-774-06) 180 ml 2018-05-01 0000-00-00 No No Current 49035-774-09 49035077409 266 mL in 1 BOTTLE, PLASTIC (49035-774-09) 266 ml 2017-08-08 0000-00-00 No No Current