FDA.reportPublic FDA data

Maximum Strength Mucus Relief DM

Product NDC
49035-839
11-digit product format
490350839
Labeler code
49035
Product ID
49035-839_42354dff-5596-9b10-e063-6294a90a74bd
Type
HUMAN OTC DRUG
Nonproprietary name
Dextromethorphan hydrobromide and Guaifenesin
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
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
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Maximum Strength Mucus Relief DM
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DEXTROMETHORPHAN HYDROBROMIDE20 mg/20mL
GUAIFENESIN400 mg/20mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9D2RTI9KYH, 495W7451VQ
Rxcui1020138

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
4fe95224-f543-4dbb-9445-8cca122b48c8Product name120150609
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
106ff02a-57e1-4c4c-a307-fd582ff4e311Product name120150212

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-839-06Maximum Strength Mucus Relief DM180 mL in 1 BOTTLELIQUID1808

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49035-839-06ML - Milliliter49035-839e223da5f-92d5-4967-b915-8260ef221b6212024-05-16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-839MAXIMUM STRENGTH MUCUS RELIEF DM (DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN) LIQUID [WAL-MART STORES,INC.,]7Current NDC, Legacy NDC, 1 package rows20241116_a748d5ab-901c-47bb-8437-997542ecebfe.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1020138dextromethorphan HBr 20 MG / guaiFENesin 400 MG in 20 mL Oral SolutionPSNa748d5ab-901c-47bb-8437-997542ecebfe8
1020138dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML Oral SolutionSCDa748d5ab-901c-47bb-8437-997542ecebfe8
1020138dextromethorphan HBr 20 MG / guaifenesin 400 MG per 20 ML Oral SolutionSYa748d5ab-901c-47bb-8437-997542ecebfe8
1020138dextromethorphan HBr 5 MG / guaifenesin 100 MG per 5 ML Oral SolutionSYa748d5ab-901c-47bb-8437-997542ecebfe8

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49035-839-0649035083906180 mL in 1 BOTTLE (49035-839-06) 180 ml2018-05-010000-00-00NoNoCurrent