SENNA-LAX is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Directrx. The primary component is Sennosides A And B.
| Product ID | 61919-205_83877e2d-7dfe-d563-e053-2991aa0a96e3 |
| NDC | 61919-205 |
| Product Type | Human Otc Drug |
| Proprietary Name | SENNA-LAX |
| Generic Name | Senna-lax |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2015-01-01 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part334 |
| Labeler Name | DirectRX |
| Substance Name | SENNOSIDES A AND B |
| Active Ingredient Strength | 9 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2015-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part334 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-01-01 |
| Marketing Category | OTC monograph not final |
| Application Number | part334 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-01-01 |
| Ingredient | Strength |
|---|---|
| SENNOSIDES A AND B | 8.6 mg/1 |
| SPL SET ID: | bbff9b05-4864-4211-95cc-94e1f30d6fd5 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0904-6522 | Senna-Lax | Sennosides |
| 15127-105 | Senna-Lax | Sennosides |
| 53041-159 | Senna-Lax | Sennosides |
| 55154-7643 | Senna-Lax | Sennosides |
| 55700-128 | Senna-Lax | SENNOSIDES A AND B |
| 55700-629 | Senna-Lax | Sennosides |
| 61919-205 | SENNA-LAX | SENNA-LAX |
| 63629-3207 | Senna-Lax | SENNOSIDES A AND B |
| 68788-6442 | Senna-Lax | Sennosides |
| 68788-9685 | Senna-Lax | Sennosides |
| 68998-373 | Senna-Lax | Sennosides |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SENNA-LAX 73470768 1460560 Live/Registered |
Nature's Herbs, Inc. 1984-03-19 |