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NDC 68788-7674-06 Stimulant Laxative Plus Stool Softener 50; 8.6 mg/1; mg/1 Details
Stimulant Laxative Plus Stool Softener 50; 8.6 mg/1; mg/1
Stimulant Laxative Plus Stool Softener is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is DOCUSATE SODIUM; SENNOSIDES.
MedlinePlus Drug Summary
Senna is used on a short-term basis to treat constipation. It also is used to empty the bowels before surgery and certain medical procedures. Senna is in a class of medications called stimulant laxatives. It works by increasing activity of the intestines to cause a bowel movement.
Related Packages: 68788-7674-06Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Senna
Stool softeners are used on a short-term basis to relieve constipation by people who should avoid straining during bowel movements because of heart conditions, hemorrhoids, and other problems. They work by softening stools to make them easier to pass.
Related Packages: 68788-7674-06Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Stool Softeners
Product Information
| NDC | 68788-7674 |
|---|---|
| Product ID | 68788-7674_920cd213-d185-4d3a-8ecf-ad9ae648bbc6 |
| Associated GPIs | 46991002770320 |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Stimulant Laxative Plus Stool Softener |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Docusate Sodium 50 mg and Sennosides 8.6 mg |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 50; 8.6 |
| Active Ingredient Units | mg/1; mg/1 |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
| Labeler Name | Preferred Pharmaceuticals, Inc. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part334 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 68788-7674-06 (68788767406)
| NDC Package Code | 68788-7674-6 |
|---|---|
| Billing NDC | 68788767406 |
| Package | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7674-6) |
| Marketing Start Date | 2020-02-28 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |