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Stool Softener
Stool Softener - 50804-005-25 - (DOCUSATE SODIUM)
Drug Information of Stool Softener
| Product NDC: | 50804-005 |
| Proprietary Name: | 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 Stool Softener
| Product NDC: | 50804-005 |
| 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: | 20100824 |
Package Information of Stool Softener
| Package NDC: | 50804-005-25 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 BOX (50804-005-25) > 25 CAPSULE in 1 BOTTLE, PLASTIC |
NDC Information of Stool Softener
| NDC Code | 50804-005-25 |
| Proprietary Name | Stool Softener |
| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (50804-005-25) > 25 CAPSULE in 1 BOTTLE, PLASTIC |
| Product NDC | 50804-005 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DOCUSATE SODIUM |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100824 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Good Sense (Geiss, Destin & Dunn, Inc.) |
| Substance Name | DOCUSATE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
