NDC 67618-300-11 - SENOKOT
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 67618-300
- Requested NDC
- 67618-300-11
- Package NDCs from labels
- 67618-300-20, 67618-300-50, 67618-300-10, 67618-300-11
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2026-09-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SENOKOT - A-S Medication Solutions | A-S Medication Solutions | 2026-09-09 | HUMAN OTC DRUG LABEL |
| Senokot (standardized senna concentrate) | Atlantis Consumer Healthcare, Inc. | 2025-12-29 | HUMAN OTC DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 67618-300-10 | Senokot | 1 in 1 CARTON | TABLET | 1 | 12 | |
| 67618-300-10 | Senokot | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | 12 | |
| 67618-300-20 | Senokot | 10 in 1 BLISTER PACK | TABLET | 10 | 12 | |
| 67618-300-20 | Senokot | 2 in 1 CARTON | TABLET | 2 | 12 | |
| 67618-300-50 | Senokot | 1 in 1 CARTON | TABLET | 1 | 12 | |
| 67618-300-50 | Senokot | 50 in 1 BOTTLE, PLASTIC | TABLET | 50 | 12 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 67618-300-10 | EA - Each | 67618-300 | 6d995b3f-8f49-4111-9050-f18f3f0be499 | 1 | 2012-07-24 |
| 67618-300-11 | EA - Each | 67618-300 | 550247ea-a7f8-4d6f-9cd9-b442d2c9f6d1 | 1 | 2012-07-24 |
| 67618-300-20 | EA - Each | 67618-300 | 029befb9-b71d-41e1-8118-4fac1a66fc44 | 1 | 2012-07-24 |
| 67618-300-40 | EA - Each | 67618-300 | 147e5b3d-423c-45e9-8222-6f15b35fc06d | 1 | 2013-06-04 |
| 67618-300-50 | EA - Each | 67618-300 | e8768eff-fab6-4153-9fa7-44686f5e8f05 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| SENNOSIDES | ACTIVE INGREDIENT | 3FYP5M0IJX | SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP] | 3 | |
| SENNOSIDES | ACTIVE MOIETY | 3FYP5M0IJX | SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP] | 3 | |
| CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS | INACTIVE INGREDIENT | L11K75P92J | SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP] | 3 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP] | 3 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP] | 3 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.