 
                        | 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 |