| Product NDC: | 36800-162 |
| Proprietary Name: | Senna S |
| Non Proprietary Name: | DOCUSATE SODIUM, SENNOSIDES |
| Active Ingredient(s): | 50; 8.6 mg/1; mg/1 & nbsp; DOCUSATE SODIUM, SENNOSIDES |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 36800-162 |
| Labeler Name: | TOP CARE (Topco Associates LLC) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130315 |
| Package NDC: | 36800-162-60 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 BOX (36800-162-60) > 60 TABLET in 1 BOTTLE, PLASTIC |
| NDC Code | 36800-162-60 |
| Proprietary Name | Senna S |
| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (36800-162-60) > 60 TABLET in 1 BOTTLE, PLASTIC |
| Product NDC | 36800-162 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DOCUSATE SODIUM, SENNOSIDES |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130315 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | TOP CARE (Topco Associates LLC) |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
| Strength Number | 50; 8.6 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |