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Stool Softener - 41520-022-01 - (docusate sodium and sennosides)

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Drug Information of Stool Softener

Product NDC: 41520-022
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: 41520-022
Labeler Name: Care One (American Sales Company)
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130301

Package Information of Stool Softener

Package NDC: 41520-022-01
Package Description: 1 BOTTLE in 1 BOX (41520-022-01) > 100 TABLET in 1 BOTTLE

NDC Information of Stool Softener

NDC Code 41520-022-01
Proprietary Name Stool Softener
Package Description 1 BOTTLE in 1 BOX (41520-022-01) > 100 TABLET in 1 BOTTLE
Product NDC 41520-022
Product Type Name HUMAN OTC DRUG
Non Proprietary Name docusate sodium and sennosides
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130301
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Care One (American Sales Company)
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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