| Product NDC: | 37205-874 |
| Proprietary Name: | LEADER Chest Congestion Relief |
| Non Proprietary Name: | Guaifenesin/phenylephrine |
| Active Ingredient(s): | 400; 10 mg/1; mg/1 & nbsp; Guaifenesin/phenylephrine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 37205-874 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060605 |
| Package NDC: | 37205-874-01 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (37205-874-01) > 50 TABLET in 1 BOTTLE, PLASTIC (37205-874-71) |
| NDC Code | 37205-874-01 |
| Proprietary Name | LEADER Chest Congestion Relief |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (37205-874-01) > 50 TABLET in 1 BOTTLE, PLASTIC (37205-874-71) |
| Product NDC | 37205-874 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin/phenylephrine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20060605 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Cardinal Health |
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 400; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |