SENNOSIDES
- Product NDC
- 49483-079
- 11-digit product format
- 494830079
- Labeler code
- 49483
- Product ID
- 49483-079_2d9b5338-d4a2-596d-e063-6294a90ac880
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SENNOSIDES
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- TIME CAP LABORATORIES, INC
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-08-30
- Substance
- SENNOSIDES A AND B
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 49483-079-00 | 302b2466d912… | e7b80fea0513… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 49483-079-01 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 49483-079-00 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 49483-079-01 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 49483-079-00 | 0efc9e666f02… | f202fb6c5f17… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 49483-079-01 | 0efc9e666f02… | f202fb6c5f17… |
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
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SENNOSIDES A AND B | 15 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1B5FPI42EN | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 200162 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 7498f5fa-1739-bb6e-e053-2a91aa0a5404 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| bee4fa8d-8d82-423a-a0b5-40a89dd13a99 | Product name | 1 | 20250618 |
| e0d2eb29-08bd-4bba-90d1-c91c68a38767 | Product name | 4 | 20250516 |
| 30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2 | Product name | 5 | 20250304 |
| 334fe8d2-68fb-4331-a576-420e302ec069 | Product name | 7 | 20240320 |
| 444b3e50-f226-46ef-bfca-2e7035d140cd | Product name | 1 | 20190611 |
| e92765c1-be81-432a-b909-1b10777ec378 | Product name | 1 | 20190208 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
| 0ca1d589-929b-4b33-bc5b-1d84abdafa6a | Product name | 1 | 20150324 |
| fc363c46-397b-4476-ac0f-70e43e8e4592 | Product name | 1 | 20150324 |
| 0441a8f5-3835-497c-aedd-bc78cba56b2a | Product name | 1 | 20150317 |
| 87711080-88eb-65c5-b2dd-bf99e700a372 | Product name | 1 | 20140508 |
| ec2149b3-5c6d-5344-f757-c86411073075 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 49483-079-00 | 2025-02-13 | 190R Sennosides tablets USP 15 mg sugar coated off-white |
| 49483-079-01 | 2025-02-13 | 190R Sennosides tablets USP 15 mg sugar coated off-white |
| 49483-079-00 | 2025-01-30 | 190R Sennosides tablets USP 15 mg sugar coated off-white |
| 49483-079-01 | 2025-01-30 | 190R Sennosides tablets USP 15 mg sugar coated off-white |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49483-079-00 | SENNOSIDES | 50000 in 1 CARTON | TABLET, SUGAR COATED | 50000 | 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 |
|---|---|---|---|---|
| 200162 | sennosides 15 MG Oral Tablet | PSN | 7498f5fa-1739-bb6e-e053-2a91aa0a5404 | 3 |
| 200162 | sennosides, USP 15 MG Oral Tablet | SCD | 7498f5fa-1739-bb6e-e053-2a91aa0a5404 | 3 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 49483-079-00 | 49483007900 | 50000 TABLET, SUGAR COATED in 1 CARTON (49483-079-00) | 2018-08-30 | 0000-00-00 | No | No | Current |
| 49483-079-01 | 49483007901 | 100 TABLET, SUGAR COATED in 1 BOTTLE, PLASTIC (49483-079-01) | 2018-08-30 | 0000-00-00 | No | No | Current |