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Gentle Stool Softener - 68016-192-25 - (DOCUSATE SODIUM)

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Drug Information of Gentle Stool Softener

Product NDC: 68016-192
Proprietary Name: Gentle Stool Softener
Non Proprietary Name: DOCUSATE SODIUM
Active Ingredient(s): 100    mg/1 & nbsp;   DOCUSATE SODIUM
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Gentle Stool Softener

Product NDC: 68016-192
Labeler Name: Chain Drug Consortium, LLC (Premier Value)
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100708

Package Information of Gentle Stool Softener

Package NDC: 68016-192-25
Package Description: 1 BOTTLE, PLASTIC in 1 BOX (68016-192-25) > 25 CAPSULE in 1 BOTTLE, PLASTIC

NDC Information of Gentle Stool Softener

NDC Code 68016-192-25
Proprietary Name Gentle Stool Softener
Package Description 1 BOTTLE, PLASTIC in 1 BOX (68016-192-25) > 25 CAPSULE in 1 BOTTLE, PLASTIC
Product NDC 68016-192
Product Type Name HUMAN OTC DRUG
Non Proprietary Name DOCUSATE SODIUM
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100708
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Chain Drug Consortium, LLC (Premier Value)
Substance Name DOCUSATE SODIUM
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Gentle Stool Softener


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