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Mucinex
Mucinex - 63824-020-66 - (acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride)
Drug Information of Mucinex
| Product NDC: | 63824-020 |
| Proprietary Name: | Mucinex |
| Non Proprietary Name: | acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride |
| Active Ingredient(s): | 650; 20; 400; 10 mg/20mL; mg/20mL; mg/20mL; mg/20mL & nbsp; acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucinex
| Product NDC: | 63824-020 |
| Labeler Name: | Reckitt Benckiser LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130331 |
Package Information of Mucinex
| Package NDC: | 63824-020-66 |
| Package Description: | 180 mL in 1 BOTTLE (63824-020-66) |
NDC Information of Mucinex
| NDC Code | 63824-020-66 |
| Proprietary Name | Mucinex |
| Package Description | 180 mL in 1 BOTTLE (63824-020-66) |
| Product NDC | 63824-020 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20130331 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Reckitt Benckiser LLC |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 650; 20; 400; 10 |
| Strength Unit | mg/20mL; mg/20mL; mg/20mL; mg/20mL |
| Pharmaceutical Classes |
