Sennosides
- Product NDC
- 51316-112
- 11-digit product format
- 513160112
- Labeler code
- 51316
- Product ID
- 51316-112_4bbdec00-ae8b-f451-e063-6294a90a0467
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sennosides
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CVS Pharmacy, Inc
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-03-23
- Substance
- SENNOSIDES
- Active strength
- 8.6 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
- Sennosides
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SENNOSIDES | 8.6 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 3FYP5M0IJX | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 312935 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 0b7736df-c7de-7d00-e063-6294a90aa57e | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 594e2c86-3079-4e6e-96c9-48f7a8afc78d | Product name | 1 | 20230718 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51316-112-02 | Sennosides | 250 in 1 BOTTLE | TABLET, FILM COATED | 250 | 3 | |
| 51316-112-03 | Sennosides | 50 in 1 BOTTLE | TABLET, FILM COATED | 50 | 3 | |
| 51316-112-03 | Sennosides | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 3 | |
| 51316-112-05 | Sennosides | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | 3 |
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 |
|---|---|---|---|---|
| 312935 | sennosides 8.6 MG Oral Tablet | PSN | 0b7736df-c7de-7d00-e063-6294a90aa57e | 3 |
| 312935 | sennosides, USP 8.6 MG Oral Tablet | SCD | 0b7736df-c7de-7d00-e063-6294a90aa57e | 3 |
| 312935 | sennosides A and B 8.6 MG Oral Tablet | SY | 0b7736df-c7de-7d00-e063-6294a90aa57e | 3 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 51316-112-02 | 51316011202 | 250 TABLET, FILM COATED in 1 BOTTLE (51316-112-02) | 2023-03-23 | No | No | Current | |
| 51316-112-03 | 51316011203 | 1 BOTTLE in 1 CARTON (51316-112-03) / 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2023-07-26 | No | No | Current |
| 51316-112-05 | 51316011205 | 500 TABLET, FILM COATED in 1 BOTTLE (51316-112-05) | 2023-12-01 | No | No | Current |