| Product NDC: | 66007-204 |
| Proprietary Name: | Expectorant plus Cough Relief |
| Non Proprietary Name: | Guaifenesin and Dextromethorphan |
| Active Ingredient(s): | 5; 100 mg/1; mg/1 & nbsp; Guaifenesin and Dextromethorphan |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GRANULE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 66007-204 |
| Labeler Name: | Capricorn Pharma Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100806 |
| Package NDC: | 66007-204-01 |
| Package Description: | 12 GRANULE in 1 CARTON (66007-204-01) |
| NDC Code | 66007-204-01 |
| Proprietary Name | Expectorant plus Cough Relief |
| Package Description | 12 GRANULE in 1 CARTON (66007-204-01) |
| Product NDC | 66007-204 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin and Dextromethorphan |
| Dosage Form Name | GRANULE |
| Route Name | ORAL |
| Start Marketing Date | 20100806 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Capricorn Pharma Inc. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 5; 100 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |