| Product NDC: | 55910-232 |
| Proprietary Name: | Mucus Relief DM Max |
| Non Proprietary Name: | Mucinex DM Max Maximum Strength |
| Active Ingredient(s): | 20; 400 mg/20mL; mg/20mL & nbsp; Mucinex DM Max Maximum Strength |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55910-232 |
| Labeler Name: | Dolgencorp, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130101 |
| Package NDC: | 55910-232-09 |
| Package Description: | 266 mL in 1 BOTTLE, PLASTIC (55910-232-09) |
| NDC Code | 55910-232-09 |
| Proprietary Name | Mucus Relief DM Max |
| Package Description | 266 mL in 1 BOTTLE, PLASTIC (55910-232-09) |
| Product NDC | 55910-232 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Mucinex DM Max Maximum Strength |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20130101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dolgencorp, Inc. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 20; 400 |
| Strength Unit | mg/20mL; mg/20mL |
| Pharmaceutical Classes |