| Product NDC: | 63941-100 |
| Proprietary Name: | Tussin Sugar Free Cough |
| Non Proprietary Name: | Dextromethorphan Hydrobromide, GUAIFENESIN, |
| Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide, GUAIFENESIN, |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63941-100 |
| Labeler Name: | Best Choice |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080924 |
| Package NDC: | 63941-100-04 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (63941-100-04) |
| NDC Code | 63941-100-04 |
| Proprietary Name | Tussin Sugar Free Cough |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (63941-100-04) |
| Product NDC | 63941-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, GUAIFENESIN, |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20080924 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Best Choice |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 10; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |