Product NDC: | 49781-017 |
Proprietary Name: | Stool Softener Plus Stimulant Laxative |
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: | 49781-017 |
Labeler Name: | Cardinal Health (Leader) 49781 |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120301 |
Package NDC: | 49781-017-56 |
Package Description: | 200 TABLET in 1 BOTTLE, PLASTIC (49781-017-56) |
NDC Code | 49781-017-56 |
Proprietary Name | Stool Softener Plus Stimulant Laxative |
Package Description | 200 TABLET in 1 BOTTLE, PLASTIC (49781-017-56) |
Product NDC | 49781-017 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DOCUSATE SODIUM, SENNOSIDES |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120301 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Cardinal Health (Leader) 49781 |
Substance Name | DOCUSATE SODIUM; SENNOSIDES |
Strength Number | 50; 8.6 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |