| Product NDC: | 30142-160 |
| Proprietary Name: | Senna- S |
| Non Proprietary Name: | docusate sodium and sennosides |
| Active Ingredient(s): | 50; 8.6 mg/1; mg/1 & nbsp; docusate sodium and sennosides |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 30142-160 |
| Labeler Name: | The Kroger Co |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100712 |
| Package NDC: | 30142-160-60 |
| Package Description: | 1 BOTTLE in 1 BOX (30142-160-60) > 60 TABLET in 1 BOTTLE |
| NDC Code | 30142-160-60 |
| Proprietary Name | Senna- S |
| Package Description | 1 BOTTLE in 1 BOX (30142-160-60) > 60 TABLET in 1 BOTTLE |
| Product NDC | 30142-160 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | docusate sodium and sennosides |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100712 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | The Kroger Co |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
| Strength Number | 50; 8.6 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |