Senna-S
- Product NDC
- 71205-970
- 11-digit product format
- 712050970
- Labeler code
- 71205
- Product ID
- 71205-970_4fa397fd-b64f-4219-962e-8d3ba9261778
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sennosides 8.6mg and Docusate Sodium 50mg
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-11-05
- 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
- Senna-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#
| Identifier | FDA.report destination |
|---|---|
| 998740 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 8678a3ee-0e2c-4c95-ad2e-83aa601f3238 | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71205-970-00 | Senna-S | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | 2 | |
| 71205-970-11 | Senna-S | 1000 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 1000 | 2 | |
| 71205-970-30 | Senna-S | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | 2 | |
| 71205-970-55 | Senna-S | 500 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 500 | 2 | |
| 71205-970-60 | Senna-S | 60 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 60 | 2 | |
| 71205-970-90 | Senna-S | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | 2 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71205-970-00 | EA - Each | 71205-970 | 74e69d17-bf29-44a9-89b6-9f89a7d23811 | 1 | 2021-10-08 |
| 71205-970-11 | EA - Each | 71205-970 | 061eed84-e4f4-410d-8eae-887958d83f11 | 1 | 2021-10-08 |
| 71205-970-30 | EA - Each | 71205-970 | 979f29e4-bbf2-442a-9303-f2cff5bbc96a | 1 | 2021-10-08 |
| 71205-970-55 | EA - Each | 71205-970 | 92be220d-95b3-44bf-979b-9e5b26d7f7de | 1 | 2021-10-08 |
| 71205-970-60 | EA - Each | 71205-970 | 8dfa4212-4ad6-486b-854e-5c7987c1dcd9 | 1 | 2021-10-08 |
| 71205-970-90 | EA - Each | 71205-970 | 5f48dda3-04b3-4bfc-b24f-bc1f726ebcde | 1 | 2021-10-08 |
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 | 8678a3ee-0e2c-4c95-ad2e-83aa601f3238 | 2 |
| 998740 | docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet | SCD | 8678a3ee-0e2c-4c95-ad2e-83aa601f3238 | 2 |
| 998740 | DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet | SY | 8678a3ee-0e2c-4c95-ad2e-83aa601f3238 | 2 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 71205-970-00 | 71205097000 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-970-00) | 2020-06-01 | 0000-00-00 | No | No | Current |
| 71205-970-11 | 71205097011 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-970-11) | 2020-06-01 | 0000-00-00 | No | No | Current |
| 71205-970-30 | 71205097030 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-970-30) | 2020-06-01 | 0000-00-00 | No | No | Current |
| 71205-970-55 | 71205097055 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-970-55) | 2020-06-01 | 0000-00-00 | No | No | Current |
| 71205-970-60 | 71205097060 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-970-60) | 2020-06-01 | 0000-00-00 | No | No | Current |
| 71205-970-90 | 71205097090 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-970-90) | 2020-06-01 | 0000-00-00 | No | No | Current |