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Stimulant laxative plus stool softener
Stimulant laxative plus stool softener - 50804-002-01 - (docusate sodium and sennosides)
Drug Information of Stimulant laxative plus stool softener
| Product NDC: | 50804-002 |
| Proprietary Name: | Stimulant laxative plus stool softener |
| 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) |
Labeler Information of Stimulant laxative plus stool softener
| Product NDC: | 50804-002 |
| Labeler Name: | Good Sense (Geiss, Destin & Dunn, Inc.) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130411 |
Package Information of Stimulant laxative plus stool softener
| Package NDC: | 50804-002-01 |
| Package Description: | 1 BOTTLE in 1 BOX (50804-002-01) > 100 TABLET in 1 BOTTLE |
NDC Information of Stimulant laxative plus stool softener
| NDC Code | 50804-002-01 |
| Proprietary Name | Stimulant laxative plus stool softener |
| Package Description | 1 BOTTLE in 1 BOX (50804-002-01) > 100 TABLET in 1 BOTTLE |
| Product NDC | 50804-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | docusate sodium and sennosides |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130411 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Good Sense (Geiss, Destin & Dunn, Inc.) |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
| Strength Number | 50; 8.6 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
