INDICATIONS & USAGE SECTION
Laxative
Sennosides 25
- Manufacturer
- Elysium Pharmaceuticals Ltd
- Effective date
- 2026-01-28
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 7
- Source
- monthly-update
- Hydrated at
- 2026-06-03 17:53:21
Label at a glance#
ProductSennosides 25
Active ingredientSENNA ALATA LEAF
Label structure3 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
Calcium sennosides 20% IH, Colloidal Silicon Di oxide USP/NF, Croscarmellose sodium USP/NF, Crospovidone [Kollidon] USP/NF, Dicalcium phosphate/ dibasic calcium phosphate [DIREC] USP/NF, Filmcoat AMB-51D0393632-Blue lake IH, Magnesium stearate. USP/NF, Microcrystalline cellulose (PH-102) USP/NF, Sodium lauryl sulfate USP/NF, Stearic acid powder USP/NF, Purified water
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Sennosides Tablets USP, 25 mg Label
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Sennosides 25
- Sennosides Tablets 25
- MAGNESIUM STEARATE
- FD&C BLUE NO. 1
- SODIUM LAURYL SULFATE
- HYPROMELLOSES
- PARAFFINUM LIQUIDUM
- CALCIUM PHOSPHATE
- MICROCRYSTALLINE CELLULOSE
- CROSCARMELLOSE SODIUM
- SILICON DIOXIDE
- POLYVINYL ALCOHOL
- SENNA ALATA LEAF
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 14803-165 | 14803-165-00 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| SODIUM LAURYL SULFATE | 368GB5141J | IACT |
| HYPROMELLOSES | 3NXW29V3WO | IACT |
| PARAFFINUM LIQUIDUM | T5L8T28FGP | IACT |
| CALCIUM PHOSPHATE | 97Z1WI3NDX | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| CROSCARMELLOSE SODIUM | M28OL1HH48 | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| POLYVINYL ALCOHOL | 532B59J990 | IACT |
| SENNA ALATA LEAF | 4BXR6YZN92 | ACTIM |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 4a3b1b61-e2f6-9231-e063-6394a90a74b4 | 4026e3db-169b-64dc-e063-6294a90a86cc | 2026-02-07 | 4026e3db-169b-64dc-e063-6294a90a86cc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.