Senokot-S
- Product NDC
- 67618-310
- 11-digit product format
- 676180310
- Labeler code
- 67618
- Product ID
- 67618-310_e5dc8b86-705c-4b54-a9fe-20d02d62ad48
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- standardized senna concentrate and docusate sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Atlantis Consumer Healthcare, Inc.
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1974-10-01
- Substance
- SENNOSIDES; DOCUSATE SODIUM
- Active strength
- 8.6; 50 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Senokot-S
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SENNOSIDES | 8.6 mg/1 |
| DOCUSATE SODIUM | 50 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 3FYP5M0IJX | Internal UNII lookup |
| F05Q2T2JA0 | Internal UNII lookup |
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| c24cdc5e-62e0-41a6-8afb-512202a569f4 | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 67618-310-01 | Senokot-S | 1 in 1 CARTON | TABLET | 1 | 11 | |
| 67618-310-01 | Senokot-S | 10 in 1 BLISTER PACK | TABLET | 10 | 11 | |
| 67618-310-30 | Senokot-S | 1 in 1 CARTON | TABLET | 1 | 11 | |
| 67618-310-30 | Senokot-S | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | 11 | |
| 67618-310-60 | Senokot-S | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | 11 | |
| 67618-310-60 | Senokot-S | 1 in 1 CARTON | TABLET | 1 | 11 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 67618-310-01 | EA - Each | 67618-310 | fca641d4-5032-4c8a-89b0-1531d188c82e | 1 | 2012-07-24 |
| 67618-310-11 | EA - Each | 67618-310 | b217ce91-d971-47fa-b151-c25b031e0673 | 1 | 2012-07-24 |
| 67618-310-30 | EA - Each | 67618-310 | 92a84d0c-0e14-4556-be2d-d25805cb714f | 1 | 2012-07-24 |
| 67618-310-60 | EA - Each | 67618-310 | d8f7c560-0b44-4674-9a72-8d1dece16702 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| up and up fiber therapy | PSYLLIUM HUSK | Target Corporation | 674753ee-1174-4c06-9ed3-a090b338a39e | 2025-11-05 | Warnings | M007 |
| up and up fiber therapy | PSYLLIUM HUSK | TARGET CORPORATION | 956c48f8-c705-4a86-9866-c68a48ddeb6c | 2025-11-05 | Warnings | M007 |
| CEO-TWO | LAXATIVE | Beutlich Pharmaceuticals, LLC | 08670636-5795-4db0-e063-6294a90afa4b | 2025-11-05 | Warnings | M007 |
| up and up gentle laxative | BISACODYL | Target Corporation | 4a29dc2b-b68f-471b-a84e-4a5096aa3748 | 2025-11-04 | Warnings | M007 |
| Target Fiber Laxative | PSYLLIUM HUSK | TARGET CORPORATION | a581116a-392d-4ac3-ae15-4318506a7b2a | 2025-11-04 | Warnings | M007 |
| up and up fiber therapy | CALCIUM POLYCARBOPHIL | Target Corporation. | e5473950-06f4-4ea4-975b-3ac94957e776 | 2025-11-04 | Warnings | M007 |
| up and up fiber therapy Natural Fiber | PSYLLIUM HUSK | Target Corporation | f8b1c831-6fd0-4a58-9726-4e0f986c8084 | 2025-11-04 | Warnings | M007 |
| OneLAX | BISACODYL | AKRON PHARMA INC | be4eeb4d-df29-45dc-94ff-933e52c8b6f6 | 2025-11-03 | Warnings | M007 |
| Gentle Stool Softener | DOCUSATE SODIUM | WALGREEN COMPANY | 169b33f9-e559-47bf-bbba-c7eda4762c7f | 2025-10-31 | Warnings | M007 |
| Senna S | DOCUSATE SODIUM, SENNOSIDES | Walgreens | 765bfd9b-7a21-4315-9add-cf13007722d5 | 2025-10-31 | Warnings | M007 |
| Gentle Stool Softener | DOCUSATE SODIUM | WALGREEN COMPANY | 71b15339-2585-4fae-8445-6fbb4f0a378e | 2025-10-31 | Warnings | M007 |
| Stool Softener Laxative | DOCUSATE SODIUM | Major Pharmaceuticals | 97561cd4-63d9-44c2-a3a3-ec668a09a4ed | 2025-10-31 | Warnings | M007 |
| Fiber Caplets | CALCIUM POLYCARBOPHIL | SAFEWAY | 08e2e8b0-90b3-48d6-a72a-40688c74771a | 2025-10-29 | Warnings | M007 |
| Glycerin | GLYCERIN | Chain Drug Marketing Association Inc. | 424d91f0-ecf9-6d9b-e063-6394a90a8006 | 2025-10-29 | Warnings | M007 |
| Publix Laxative Maximum Strength | CALCIUM SENNOSIDES | PUBLIX SUPER MARKETS, INC | 11112859-ef1e-4b37-9915-ba4d06a3f198 | 2025-10-28 | Warnings | M007 |
| Publix Stimulant Laxative | BISACODYL | PUBLIX SUPER MARKETS, INC | 02e596a7-b8e5-4f55-9bc6-6d17e0fabda7 | 2025-10-28 | Warnings | M007 |
| PUBLIX | PSYLLIUM HUSK | PUBLIX SUPER MARKETS, INC | 55f98d3f-f282-4f19-b373-0b59640d274d | 2025-10-28 | Warnings | M007 |
| PUBLIX | CALCIUM POLYCARBOPHIL | PUBLIX SUPER MARKETS, INC | 02e3f4ce-8961-425c-98a9-3b9d66709ca5 | 2025-10-28 | Warnings | M007 |
| Publix Women Laxative | BISACODYL | PUBLIX SUPER MARKETS, INC | 03eeca55-f239-4a01-a900-c1943f27a834 | 2025-10-28 | Warnings | M007 |
| Publix Fiber Therapy Orange Smooth | PSYLLIUM HUSK | PUBLIX SUPER MARKETS, INC | b9c54c20-cd82-4627-9217-a66834db4799 | 2025-10-28 | Warnings | M007 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 998740 | sennosides 8.6 MG / docusate sodium 50 MG Oral Tablet | PSN | c24cdc5e-62e0-41a6-8afb-512202a569f4 | 11 |
| 1248015 | Senokot-S 8.6 MG / 50 MG Oral Tablet | PSN | c24cdc5e-62e0-41a6-8afb-512202a569f4 | 11 |
| 1248015 | docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [SENOKOT-S] | SBD | c24cdc5e-62e0-41a6-8afb-512202a569f4 | 11 |
| 998740 | docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet | SCD | c24cdc5e-62e0-41a6-8afb-512202a569f4 | 11 |
| 998740 | DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet | SY | c24cdc5e-62e0-41a6-8afb-512202a569f4 | 11 |
| 1248015 | DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [SENOKOT-S] | SY | c24cdc5e-62e0-41a6-8afb-512202a569f4 | 11 |
| 1248015 | SENOKOT-S (docusate sodium 50 MG / sennosides, USP 8.6 MG) Oral Tablet | SY | c24cdc5e-62e0-41a6-8afb-512202a569f4 | 11 |
| 1248015 | SENOKOT-S Oral Tablet | SY | c24cdc5e-62e0-41a6-8afb-512202a569f4 | 11 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 67618-310-01 | 67618031001 | 1 BLISTER PACK in 1 CARTON (67618-310-01) / 10 TABLET in 1 BLISTER PACK | 1 blister pack | 1974-10-01 | 0000-00-00 | No | No | Current |
| 67618-310-10 | 67618031010 | 1 BOTTLE, PLASTIC in 1 CARTON (67618-310-10) / 100 TABLET in 1 BOTTLE, PLASTIC | 2026-09-30 | No | No | Current | ||
| 67618-310-30 | 67618031030 | 1 BOTTLE, PLASTIC in 1 CARTON (67618-310-30) / 30 TABLET in 1 BOTTLE, PLASTIC | 1974-10-01 | 0000-00-00 | No | No | Current | |
| 67618-310-60 | 67618031060 | 1 BOTTLE, PLASTIC in 1 CARTON (67618-310-60) / 60 TABLET in 1 BOTTLE, PLASTIC | 1974-10-01 | 0000-00-00 | No | No | Current |