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Up and up stool softener
Up and up stool softener - 11673-486-78 - (Docusate sodium)
Drug Information of Up and up stool softener
| Product NDC: | 11673-486 |
| Proprietary Name: | Up and up stool softener |
| Non Proprietary Name: | Docusate sodium |
| Active Ingredient(s): | 100 mg/1 & nbsp; Docusate sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Up and up stool softener
| Product NDC: | 11673-486 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090708 |
Package Information of Up and up stool softener
| Package NDC: | 11673-486-78 |
| Package Description: | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (11673-486-78) |
NDC Information of Up and up stool softener
| NDC Code | 11673-486-78 |
| Proprietary Name | Up and up stool softener |
| Package Description | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (11673-486-78) |
| Product NDC | 11673-486 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Docusate sodium |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20090708 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Target Corporation |
| Substance Name | DOCUSATE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
