FDA.reportPublic FDA data

MUCUS RELIEF DM

Product NDC
41226-280
Requested package NDC
41226-280-03
11-digit product format
412260280
Labeler code
41226
Product ID
41226-280_89697bdd-6c45-47bf-e053-2a95a90aa0ca
Type
HUMAN OTC DRUG
Nonproprietary name
DEXTROMETHORPHAN HBR/GUAIFENESIN
Dosage form
TABLET
Route
ORAL
Labeler
KROGER COMPANY
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2019-06-03
Substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength
20; 400 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

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MUCUS RELIEF DMDEXTROMETHORPHAN HBR/GUAIFENESINKROGER COMPANY813baf42-edb0-33a9-e053-2a91aa0a85992019-05-21WarningsExact identifier
ndc (package): 41226-280-03
ndc (product): 41226-280
ndc11 (package): 41226028003

Additional Listing Data#

Finished product
Yes
Brand name base
MUCUS RELIEF DM
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DEXTROMETHORPHAN HYDROBROMIDE20 mg/1
GUAIFENESIN400 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9D2RTI9KYHInternal UNII lookup
495W7451VQInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1147685Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
813baf42-edb0-33a9-e053-2a91aa0a8599Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bf324df6-7127-7deb-def5-2681c136cd03Product name320250325
43a1ed49-eae2-4840-8075-cb4b33478540Product name120230425
ba088a92-ab5e-b2d4-e908-f5ea691b7587Product name720210201
4fe95224-f543-4dbb-9445-8cca122b48c8Product name120150609
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
106ff02a-57e1-4c4c-a307-fd582ff4e311Product name120150212
76633df9-0d59-4b88-03ed-21dee1b966f8Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41226-280-03MUCUS RELIEF DM30 in 1 BOTTLETABLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41226-280MUCUS RELIEF DM (DEXTROMETHORPHAN HBR/GUAIFENESIN) TABLET [KROGER COMPANY]2Current NDC, Legacy NDC, 1 package rows20190603_813baf42-edb0-33a9-e053-2a91aa0a8599.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1147685dextromethorphan HBr 20 MG / guaiFENesin 400 MG Oral TabletPSN813baf42-edb0-33a9-e053-2a91aa0a85992
1147685dextromethorphan hydrobromide 20 MG / guaifenesin 400 MG Oral TabletSCD813baf42-edb0-33a9-e053-2a91aa0a85992
1147685guaifenesin 400 MG / dextromethorphan HBr 20 MG Oral TabletSY813baf42-edb0-33a9-e053-2a91aa0a85992

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41226-280-034122602800330 TABLET in 1 BOTTLE (41226-280-03) 30 tablet2019-06-030000-00-00NoNoCurrent