NDC 17856-1127-01 - OneLAX SENNA
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 17856-1127
- Requested NDC
- 17856-1127-01
- Package NDCs from labels
- 17856-1127-5, 17856-1127-1, 17856-1127-6, 17856-1127-2, 17856-1127-7, 17856-1127-3, 17856-1127-8, 17856-1127-4, 17856-1127-9, 17856-1127-01
- Manufacturer
- ATLANTIC BIOLOGICALS CORP.
- Effective date
- 2025-12-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OneLAX SENNA SYRUP Natural Vegitable Lexative Natural Choclate Flavor | ATLANTIC BIOLOGICALS CORP. | 2025-12-29 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17856-1127-1 | OneLAX SENNA | 120 in 1 BOX, UNIT-DOSE | SYRUP | 120 | 4 | |
| 17856-1127-2 | OneLAX SENNA | 72 in 1 BOX, UNIT-DOSE | SYRUP | 72 | 4 | |
| 17856-1127-3 | OneLAX SENNA | 72 in 1 BOX, UNIT-DOSE | SYRUP | 72 | 4 | |
| 17856-1127-4 | OneLAX SENNA | 72 in 1 BOX, UNIT-DOSE | SYRUP | 72 | 4 | |
| 17856-1127-5 | OneLAX SENNA | 2.5 mL in 1 SYRINGE | SYRUP | 2.5 | 4 | |
| 17856-1127-6 | OneLAX SENNA | 5 mL in 1 CUP, UNIT-DOSE | SYRUP | 5 | 4 | |
| 17856-1127-7 | OneLAX SENNA | 10 mL in 1 CUP, UNIT-DOSE | SYRUP | 10 | 4 | |
| 17856-1127-8 | OneLAX SENNA | 15 mL in 1 CUP, UNIT-DOSE | SYRUP | 15 | 4 | |
| 17856-1127-9 | OneLAX SENNA | 120 in 1 BOX, UNIT-DOSE | SYRUP | 120 | 4 | |
| 17856-1127-9 | OneLAX SENNA | 2.5 mL in 1 SYRINGE | SYRUP | 2.5 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17856-1127 | ONELAX SENNA (SENNA) SYRUP [ATLANTIC BIOLOGICALS CORP.] | 2 | Current NDC, 10 package rows | 20250525_d2a5a13a-e7e4-488a-b60b-4dd467efa971.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 17856-1127-1 | ML - Milliliter | 17856-1127 | c08714e3-905e-4e20-97c1-043685cae097 | 1 | 2024-06-10 |
| 17856-1127-2 | ML - Milliliter | 17856-1127 | 66cf67fe-098b-44ed-af11-ea6e69bd17a7 | 1 | 2024-06-10 |
| 17856-1127-3 | ML - Milliliter | 17856-1127 | e067a394-8c02-4ce9-a6a7-be9ca07d796c | 1 | 2024-06-10 |
| 17856-1127-4 | ML - Milliliter | 17856-1127 | c419747c-7cee-4a84-a0ab-0b787a395329 | 1 | 2024-06-10 |
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 |
|---|---|---|---|---|---|---|
| Rite Aid Fiber Caplets | CALCIUM POLYCARBOPHIL | RITE AID CORPORATION | 06e46cb0-2928-479e-984d-2305fff995e0 | 2024-10-30 | Warnings | M007 |
| Premier Value Orange Flavor | PSYLLIUM HUSK | PHARMACY VALUE ALLIANCE, LLC | 2d580965-2bef-46ee-8532-fbe34330a4b4 | 2024-10-28 | Warnings | M007 |
| Premier Value Fiber Therapy | METHYLCELLULOSE | PHARMACY VALUE ALLIANCE, LLC | b875d5f8-02f3-4474-9fda-83091bc7de04 | 2024-10-28 | Warnings | M007 |
| Premier Value Fiber Therapy Original Coarse | PSYLLIUM HUSK | PHARMACY VALUE ALLIANCE, LLC | 8c85a13d-ae99-4599-9a28-c3965caa6376 | 2024-10-28 | Warnings | M007 |
| Premier Value | CALCIUM POLYCARBOPHIL | PHARMACY VALUE ALLIANCE, LLC | 4d766548-00d0-41bd-bb58-b69e037c77e2 | 2024-10-28 | Warnings | M007 |
| Lactistat | ARSENICUM ALBUM, CALCAREA CARBONICA, COCCULUS INDICUS, GRAPHITES, HYDROFLUORICUM ACIDUM, LACHESIS MUTUS, LACTICUM ACIDUM, RHUS TOX, RUTA GRAVEOLENS, SARCOLACTICUM ACIDUM, SACCHARUM OFFICINALE | Energique, Inc. | 8dcc4a3a-9f21-4a77-ae42-b2c8283a076a | 2024-10-28 | Warnings | C151H8M554 |
| Premier Value Fiber | PSYLLIUM HUSK | Chain Drug Consortium, LLC | c507fe4a-1f8e-4780-a2f5-9da6e5922bef | 2024-10-28 | Warnings | M007 |
| Premier Value Fiber Therapy Orange Flavor | PSYLLIUM HUSK | PHARMACY VALUE ALLIANCE, LLC | 85651bd7-e959-4455-a5ed-bd0223ce0563 | 2024-10-28 | Warnings | M007 |
| Stool Softener | DOCUSATE SODIUM AND SENNOSIDES | BETTER LIVING BRANDS LLC. | f2c61c71-9a23-4bd3-e053-2a95a90ad460 | 2024-10-26 | Warnings | M007 |
| Grain and Seed Antigens | BAMBOO, BARLEY, CORN, COTTON SEED, FLAX SEED (LINUM USITATISSIMUM), MILLET, MILO, OAT, POPPY SEED, RICE, RYE, SAFFLOWER, SESAME, SORGHUM, SOY BEAN, SUGARCANE, SUNFLOWER (HELIANTHUS ANNUUS), WHEAT, ARSENICUM ALBUM, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, SULPHUR | Energique, Inc. | a028eaea-76ef-45db-80e1-d7b4a0655d5e | 2024-10-25 | Warnings | C151H8M554 |
| Pedia-Lax | GLYCERIN | C.B. Fleet Company, Inc. | ae367381-7146-4307-823d-2bb44c1d4200 | 2024-10-25 | Warnings | M007 |
| Epsom Salt | MAGNESIUM SULFATE | Target Corporation | f7309f4a-f1f5-420e-bfc7-fb4495a5afba | 2024-10-24 | Warnings | M007 |
| Epsom Salt | MAGNESIUM SULFATE | Target Corporation | 2540ae39-2218-0f6a-e063-6294a90a5efc | 2024-10-24 | Warnings | M007 |
| DOCUSATE SODIUM | DOCUSATE SODIUM | Sam's West Inc | b0e99ebb-41fc-459f-86d2-f0e3527f97b0 | 2024-10-24 | Warnings | M007 |
| Stool Softener | DOCUSATE SODIUM | A-S Medication Solutions | ef05ad45-7082-43e6-9533-a79c5aa0f373 | 2024-10-22 | Warnings | M007 |
| Senna Syrup | SENNOSIDES | Rising Pharma Holdings, Inc. | dc636b83-6eca-412e-bac5-0c736b371ca7 | 2024-10-18 | Warnings | 702311 |
| Bliss GVS Children | GLYCERIN | Bliss GVS Pharma Limited | 03237ed2-265f-4acd-b504-d82b9263287c | 2024-10-17 | Warnings | M007 |
| NATURAL Epsom Salt | MAGNESIUM SULFATE | Universal Distribution Center LLC | b2682e51-ffa4-4556-b2a6-b0dbd543fd4f | 2024-10-16 | Warnings | M007 |
| EyS Eye Wash | WATER | Eyes-Plus LLC | 1443f6bf-3a77-4a19-8585-0ec58efe042f | 2024-10-15 | Warnings | 059QF0KO0R |
| Eye Wash | WATER SOLUTION | Kroger Company | 354402ad-581d-47e7-9fd3-933bef281ff4 | 2024-10-11 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.