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Tussin CF Multi-Symptom Cold
Tussin CF Multi-Symptom Cold - 53942-504-26 - (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE)
Drug Information of Tussin CF Multi-Symptom Cold
| Product NDC: | 53942-504 |
| Proprietary Name: | Tussin CF Multi-Symptom Cold |
| Non Proprietary Name: | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient(s): | 10; 100; 5 mg/5mL; mg/5mL; mg/5mL & nbsp; DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tussin CF Multi-Symptom Cold
| Product NDC: | 53942-504 |
| Labeler Name: | DeMoulas Market Basket |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120920 |
Package Information of Tussin CF Multi-Symptom Cold
| Package NDC: | 53942-504-26 |
| Package Description: | 237 mL in 1 BOTTLE (53942-504-26) |
NDC Information of Tussin CF Multi-Symptom Cold
| NDC Code | 53942-504-26 |
| Proprietary Name | Tussin CF Multi-Symptom Cold |
| Package Description | 237 mL in 1 BOTTLE (53942-504-26) |
| Product NDC | 53942-504 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120920 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | DeMoulas Market Basket |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10; 100; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
