United States· US:71335-2693_1502a2b6-0ef3-40ca-820a-b9ff835cad03
Stimulant Laxative Plus Stool Softener
A medicinal product containing sennosides; docusate sodium, registered in United States by Bryant Ranch Prepack.
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; DOCUSATE SODIUM
- Manufacturer
- Bryant Ranch Prepack
- 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 · 18
- ndc1171335-2693-1
- ndc1171335-2693-2
- ndc1171335-2693-3
- ndc1171335-2693-4
- ndc1171335-2693-5
- ndc1171335-2693-6
- ndc1171335-2693-7
- ndc1171335-2693-8
- ndc1171335-2693-9
- ndc11713352693130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2693-1)
- ndc117133526932120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2693-2)
- ndc11713352693360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2693-3)
- ndc11713352693490 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2693-4)
- ndc117133526935100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2693-5)
- ndc11713352693628 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2693-6)
- ndc11713352693756 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2693-7)
- ndc11713352693814 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2693-8)
- ndc11713352693920 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2693-9)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Sennosides; docusate sodium in 1 other country
What each register calls a product with the same active substance — salts and hydrates count as the same.
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/06177f2f-08ed-4a4f-91a2-4fdb6c044cff GET /v1/drugs/06177f2f-08ed-4a4f-91a2-4fdb6c044cff?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; 50",
"substance": "SENNOSIDES; DOCUSATE SODIUM",
"productndc": "71335-2693",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"strength_unit": "mg/1; mg/1",
"application_number": "M007",
"marketing_category": "OTC MONOGRAPH DRUG"
}See everything about sennosides; docusate sodium.
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.