 
                        | Product NDC: | 63824-014 | 
| Proprietary Name: | Mucinex Fast-Max | 
| Non Proprietary Name: | dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride | 
| Active Ingredient(s): | 20; 400; 10 mg/20mL; mg/20mL; mg/20mL & nbsp; dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 63824-014 | 
| Labeler Name: | Reckitt Benckiser LLC | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20120207 | 
| Package NDC: | 63824-014-66 | 
| Package Description: | 180 mL in 1 BOTTLE (63824-014-66) | 
| NDC Code | 63824-014-66 | 
| Proprietary Name | Mucinex Fast-Max | 
| Package Description | 180 mL in 1 BOTTLE (63824-014-66) | 
| Product NDC | 63824-014 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride | 
| Dosage Form Name | SOLUTION | 
| Route Name | ORAL | 
| Start Marketing Date | 20120207 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | Reckitt Benckiser LLC | 
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE | 
| Strength Number | 20; 400; 10 | 
| Strength Unit | mg/20mL; mg/20mL; mg/20mL | 
| Pharmaceutical Classes |