FDA.reportPublic FDA data

Mucus Relief

Product NDC
46122-790
11-digit product format
461220790
Labeler code
46122
Product ID
46122-790_4b050df4-4ebb-4716-bc39-362df2ed7424
Type
HUMAN OTC DRUG
Nonproprietary name
Dextromethorphan HBr, Guaifenesin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Amerisource Bergen
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-07-23
Substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength
20; 400 mg/1; mg/1
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
Mucus Relief
Brand name suffix
DM Cough
Listing expiration
2026-12-31

Active Ingredients#

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

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9D2RTI9KYH, 495W7451VQ
Rxcui1147685

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
46122-790-61Mucus ReliefDM Cough1 in 1 CARTONTABLET, FILM COATED13
46122-790-61Mucus ReliefDM Cough50 in 1 BOTTLE, PLASTICTABLET, FILM COATED503

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
46122-790-61EA - Each46122-79013582038-9201-4859-99b0-67a0674084fe12025-03-04

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
46122-790MUCUS RELIEF DM COUGH (DEXTROMETHORPHAN HBR, GUAIFENESIN) TABLET, FILM COATED [AMERISOURCE BERGEN]2Current NDC, 2 package rows20240724_639a59b7-ccff-485e-a232-38b680827229.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1147685dextromethorphan HBr 20 MG / guaiFENesin 400 MG Oral TabletPSN639a59b7-ccff-485e-a232-38b6808272293
1147685dextromethorphan hydrobromide 20 MG / guaifenesin 400 MG Oral TabletSCD639a59b7-ccff-485e-a232-38b6808272293
1147685guaifenesin 400 MG / dextromethorphan HBr 20 MG Oral TabletSY639a59b7-ccff-485e-a232-38b6808272293

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
46122-790-61461220790611 BOTTLE, PLASTIC in 1 CARTON (46122-790-61) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC2024-07-23NoNoHistorical