Mucus Relief DM
- Product NDC
- 41250-533
- 11-digit product format
- 412500533
- Labeler code
- 41250
- Product ID
- 41250-533_462149db-00f4-4a0a-b9c9-1b63c07f2db6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr and Guaifenesin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2005-12-31
- Marketing end
- 2027-11-30
- 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
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mucus Relief DM
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEXTROMETHORPHAN HYDROBROMIDE | 20 mg/1 |
| GUAIFENESIN | 400 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9D2RTI9KYH, 495W7451VQ |
| Rxcui | 1147685 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41250-533-11 | Mucus Relief DM | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 16 |
| 41250-533-11 | Mucus Relief DM | 60 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 60 | | 16 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| DEXTROMETHORPHAN HYDROBROMIDE | ACTIVE INGREDIENT | 9D2RTI9KYH | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
| GUAIFENESIN | ACTIVE INGREDIENT | 495W7451VQ | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
| DEXTROMETHORPHAN | ACTIVE MOIETY | 7355X3ROTS | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
| GUAIFENESIN | ACTIVE MOIETY | 495W7451VQ | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
| D&C YELLOW NO. 10 | INACTIVE INGREDIENT | 35SW5USQ3G | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
| MALTODEXTRIN | INACTIVE INGREDIENT | 7CVR7L4A2D | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUIAFENESIN) TABLET, FILM COATED [MEIJER] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41250-533 | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUAIFENESIN) TABLET, FILM COATED [MEIJER DISTRIBUTION INC] | 15 | Current NDC, Legacy NDC, 2 package rows | 20241206_8ed5b802-a26e-45b4-a696-bc64dbac4733.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-533-11 | 41250053311 | 1 BOTTLE, PLASTIC in 1 CARTON (41250-533-11) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2005-12-31 | 2027-11-30 | No | No | Current |