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Stimulant laxative plus stool softener - 50804-002-01 - (docusate sodium and sennosides)

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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

Complete Information of Stimulant laxative plus stool softener


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