United States· US:72090-031_ae68255e-6cc3-4ab6-bee0-373fbffcc1f0
Senna Natural Relief
A medicinal product containing sennosides, registered in United States by Pioneer Life Sciences, LLC.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- SENNOSIDES
- Manufacturer
- Pioneer Life Sciences, LLC
- Country
- United States (US)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc1172090-031-60
- ndc117209003160600 TABLET in 1 BOTTLE (72090-031-60)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Sennosides in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomCenlax 7.5mg tablets 12 Years PlusManx Healthcare Ltd
- SpainLAXANTE SALUD 7,5 MG COMPRIMIDOS RECUBIERTOS CON PELÍCULAPharmaceutical Innovation Services S.L.
- NetherlandsX-Praep stroop 2 mg/mlEuro Registratie Collectief B.V.
- FrancePURSENNIDE 20 mg, comprimé enrobéHALEON FRANCE
- IrelandSenokot 7.5 mg/5 ml SyrupReckitt Benckiser Ireland Ltd
- NorwayPursennidHaleon Denmark ApS
- SwedenPursennid Ex-Lax 12 mg Dragerad tablettHaleon Denmark ApS
- FinlandExprepMundipharma Oy
Authorised across Europe · EMA
The same active substance is authorised in 10 EEA countries. Names it is sold under:
- Cyprus · Senna Remedica
- Finland · Pursennid Ex Lax, Pursennid Ex-Lax
- France · Pursennide
- United Kingdom (Northern Ireland) · Sennosides 12 Years Plus Crescent Pharma, Sennosides 12 Years Plus Farmak Pharmaceuticals Uk
- Ireland · Senokot
- Italy · Pursennid
- Malta · Senna
- Norway · Pursennid
- Portugal · Pursennide
- Sweden · Pursennid Ex-Lax
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/0e33cfd8-3ece-44fe-9867-76b5d91cceb3 GET /v1/drugs/0e33cfd8-3ece-44fe-9867-76b5d91cceb3?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"route": "ORAL",
"source": "ndc",
"strength": "8.6",
"substance": "SENNOSIDES",
"productndc": "72090-031",
"dosage_form": "TABLET",
"dea_schedule": null,
"strength_unit": "mg/1",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG"
}See everything about sennosides.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.