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Stool Softener - 36800-003-01 - (docusate sodium and sennosides)

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Drug Information of Stool Softener

Product NDC: 36800-003
Proprietary Name: 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 Stool Softener

Product NDC: 36800-003
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: 20100709

Package Information of Stool Softener

Package NDC: 36800-003-01
Package Description: 1 BOTTLE in 1 BOX (36800-003-01) > 100 TABLET in 1 BOTTLE

NDC Information of Stool Softener

NDC Code 36800-003-01
Proprietary Name Stool Softener
Package Description 1 BOTTLE in 1 BOX (36800-003-01) > 100 TABLET in 1 BOTTLE
Product NDC 36800-003
Product Type Name HUMAN OTC DRUG
Non Proprietary Name docusate sodium and sennosides
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100709
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

Complete Information of Stool Softener


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