FDA.reportPublic FDA data

Mucus DM

Product NDC
11822-5050
11-digit product format
118225050
Labeler code
11822
Product ID
11822-5050_5f18f89e-2025-4c8c-8985-db91787f985b
Type
HUMAN OTC DRUG
Nonproprietary name
Dextromethorphan Hydrobromide Guaifenesin
Dosage form
LIQUID
Route
ORAL
Labeler
Rite Aid Corporation
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-09-30
Marketing end
2026-09-30
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
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Mucus DM

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
4fe95224-f543-4dbb-9445-8cca122b48c8Product name120150609
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
106ff02a-57e1-4c4c-a307-fd582ff4e311Product name120150212

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-5050-62023-02-20C16284748780-1d6a99b39-6b0e-a426-e053-dadaa90af4c2Drug Facts
11822-5050-62022-01-28C16284748780-1d6a99b39-6b0e-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-5050-6Mucus DM177 mL in 1 BOTTLE, PLASTICLIQUID1774

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-5050MUCUS DM (DEXTROMETHORPHAN HYDROBROMIDE GUAIFENESIN) LIQUID [RITE AID CORPORATION]3Current NDC, Legacy NDC, 1 package rows20240509_b1c9a009-92e7-4a85-b1b0-51d86156d882.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1020138dextromethorphan HBr 20 MG / guaiFENesin 400 MG in 20 mL Oral SolutionPSNb1c9a009-92e7-4a85-b1b0-51d86156d8824
1020138dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML Oral SolutionSCDb1c9a009-92e7-4a85-b1b0-51d86156d8824
1020138dextromethorphan HBr 20 MG / guaifenesin 400 MG per 20 ML Oral SolutionSYb1c9a009-92e7-4a85-b1b0-51d86156d8824
1020138dextromethorphan HBr 5 MG / guaifenesin 100 MG per 5 ML Oral SolutionSYb1c9a009-92e7-4a85-b1b0-51d86156d8824

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-5050-611822505006177 mL in 1 BOTTLE, PLASTIC (11822-5050-6) 177 ml2019-09-302026-09-30NoNoCurrent