| Product NDC: | 10956-788 |
| Proprietary Name: | Refenesen Chest Congestion Relief |
| Non Proprietary Name: | Guaifenesin |
| Active Ingredient(s): | 400 mg/1 & nbsp; Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10956-788 |
| Labeler Name: | Reese Pharmaceutical Co |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030923 |
| Package NDC: | 10956-788-01 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (10956-788-01) > 100 TABLET in 1 BOTTLE, PLASTIC (10956-788-09) |
| NDC Code | 10956-788-01 |
| Proprietary Name | Refenesen Chest Congestion Relief |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (10956-788-01) > 100 TABLET in 1 BOTTLE, PLASTIC (10956-788-09) |
| Product NDC | 10956-788 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20030923 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Reese Pharmaceutical Co |
| Substance Name | GUAIFENESIN |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |