COUGH BE GONE is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Rfx Pharmaceutical Co., Ltd.. The primary component is Dextromethorphan Hydrobromide; Guaifenesin.
| Product ID | 76206-001_533bb57a-b5dc-4527-a92a-6644617e265d | 
| NDC | 76206-001 | 
| Product Type | Human Otc Drug | 
| Proprietary Name | COUGH BE GONE | 
| Generic Name | Dextromethorphan Hydrobromide Guaifenesin | 
| Dosage Form | Liquid | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2014-01-30 | 
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL | 
| Application Number | part341 | 
| Labeler Name | RFX Pharmaceutical Co., Ltd. | 
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN | 
| Active Ingredient Strength | 20 mg/10mL; mg/10mL | 
| NDC Exclude Flag | E | 
| Listing Certified Through | 2018-12-31 | 
| Marketing Start Date | 2014-01-30 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | OTC monograph final | 
| Application Number | part341 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2014-01-30 | 
| Marketing Category | OTC monograph final | 
| Application Number | part341 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2014-01-30 | 
| Inactivation Date | 2020-01-31 | 
| Reactivation Date | 2020-03-03 | 
| Ingredient | Strength | 
|---|---|
| DEXTROMETHORPHAN HYDROBROMIDE | 20 mg/10mL | 
| SPL SET ID: | 89a5588f-a6a6-40dd-b96f-79bd3ea9e31f | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 75663-001 | COUGH BE GONE | Dextromethorphan Hydrobromide Guaifenesin | 
| 76206-001 | COUGH BE GONE | Dextromethorphan Hydrobromide Guaifenesin | 
| 11822-5050 | Mucus DM | Dextromethorphan Hydrobromide Guaifenesin | 
| 30142-508 | Mucus Relief DM | Dextromethorphan Hydrobromide Guaifenesin | 
| 69842-904 | Mucus Relief DM | Dextromethorphan Hydrobromide Guaifenesin |