Mucus Relief DM

Product NDC
49035-960
11-digit product format
490350960
Labeler code
49035
Product ID
49035-960_249e65f5-a8a0-4e4a-8caa-fca3448e9e95
Type
HUMAN OTC DRUG
Nonproprietary name
Guaifenesin and Dextromethorphan HBr
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Wal-Mart Stores, Inc.
Application
ANDA206941
Marketing category
ANDA
Marketing start
2017-03-17
Substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength
30; 600 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 DM
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DEXTROMETHORPHAN HYDROBROMIDE30 mg/1
GUAIFENESIN600 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9D2RTI9KYH, 495W7451VQ
Rxcui1298324

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
49035-960-12Mucus Relief DM1 in 1 CARTONTABLET, EXTENDED RELEASE17
49035-960-12Mucus Relief DM40 in 1 BOTTLETABLET, EXTENDED RELEASE407
49035-960-73Mucus Relief DM1 in 1 CARTONTABLET, EXTENDED RELEASE17
49035-960-73Mucus Relief DM20 in 1 BOTTLETABLET, EXTENDED RELEASE207

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49035-960-12EA - Each49035-9604c6a1382-7337-4a9c-a7d8-f0dceb54fd6c12024-04-05
49035-960-73EA - Each49035-960f8772aea-70b8-48f2-aed7-cbc250da5deb12019-12-10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-960MUCUS RELIEF DM (GUAIFENESIN AND DEXTROMETHORPHAN HBR) TABLET, EXTENDED RELEASE [WAL-MART STORES, INC.]7Current NDC, Legacy NDC, 4 package rows20240210_48ecf1f4-0571-4d7e-b0cc-309c88b7f1bf.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1298324guaiFENesin 600 MG / dextromethorphan HBr 30 MG 12HR Extended Release Oral TabletPSN48ecf1f4-0571-4d7e-b0cc-309c88b7f1bf7
129832412 HR dextromethorphan hydrobromide 30 MG / guaifenesin 600 MG Extended Release Oral TabletSCD48ecf1f4-0571-4d7e-b0cc-309c88b7f1bf7
1298324dextromethorphan hydrobromide 30 MG / guaifenesin 600 MG 12 HR Extended Release Oral TabletSY48ecf1f4-0571-4d7e-b0cc-309c88b7f1bf7

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49035-960-12490350960121 BOTTLE in 1 CARTON (49035-960-12) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE1 bottle2017-03-170000-00-00NoNoCurrent
49035-960-73490350960731 BOTTLE in 1 CARTON (49035-960-73) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE1 bottle2017-03-170000-00-00NoNoCurrent