Quality Choice Mucus Relief DM

Product NDC
63868-753
11-digit product format
638680753
Labeler code
63868
Product ID
63868-753_07b36c8b-1869-45d2-90be-b40b0fdb4f65
Type
HUMAN OTC DRUG
Nonproprietary name
Dextromethorphan Hydrobromide / Guaifenesin
Dosage form
TABLET
Route
ORAL
Labeler
Chain Drug Marketing Association
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2012-08-01
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
Quality Choice Mucus Relief DM
Brand name suffix
DM
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
63868-753-50Quality Choice Mucus Relief DMDM1 in 1 CARTONTABLET14
63868-753-50Quality Choice Mucus Relief DMDM50 in 1 BOTTLETABLET504

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63868-753-50EA - Each63868-753dc57160c-56ba-446f-a518-02544cb19d9612015-10-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DEXTROMETHORPHAN HYDROBROMIDEACTIVE INGREDIENT9D2RTI9KYHQUALITY CHOICE MUCUS RELIEF DM DM (DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]1
GuaifenesinACTIVE INGREDIENT495W7451VQQUALITY CHOICE MUCUS RELIEF DM DM (DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]1
DEXTROMETHORPHANACTIVE MOIETY7355X3ROTSQUALITY CHOICE MUCUS RELIEF DM DM (DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]1
GuaifenesinACTIVE MOIETY495W7451VQQUALITY CHOICE MUCUS RELIEF DM DM (DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UQUALITY CHOICE MUCUS RELIEF DM DM (DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30QUALITY CHOICE MUCUS RELIEF DM DM (DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]1
MALTODEXTRININACTIVE INGREDIENT7CVR7L4A2DQUALITY CHOICE MUCUS RELIEF DM DM (DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4QUALITY CHOICE MUCUS RELIEF DM DM (DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]1
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APQUALITY CHOICE MUCUS RELIEF DM DM (DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63868-753QUALITY CHOICE MUCUS RELIEF DM DM (DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]4Current NDC, Legacy NDC, 2 package rows20241220_1c33a01f-1186-4a19-b639-a9cd49245220.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1147685dextromethorphan HBr 20 MG / guaiFENesin 400 MG Oral TabletPSN1c33a01f-1186-4a19-b639-a9cd492452204
1147685dextromethorphan hydrobromide 20 MG / guaifenesin 400 MG Oral TabletSCD1c33a01f-1186-4a19-b639-a9cd492452204
1147685guaifenesin 400 MG / dextromethorphan HBr 20 MG Oral TabletSY1c33a01f-1186-4a19-b639-a9cd492452204

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63868-753-50638680753501 BOTTLE in 1 CARTON (63868-753-50) / 50 TABLET in 1 BOTTLE1 bottle2012-08-010000-00-00NoNoCurrent