United States · FDA National Drug Code directory
Senna-S
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 71205-970_4fa397fd-b64f-4219-962e-8d3ba9261778
- Product NDC
- 71205-970
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sennosides 8.6mg and Docusate Sodium 50mg
- Labeler
- Proficient Rx LP
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20181105
- Source listing expiry
- 20261231
Source-listed ingredients
- SENNOSIDES — 8.6 mg/1
- DOCUSATE SODIUM — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-970-00) · 71205-970-00
- 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-970-11) · 71205-970-11
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-970-30) · 71205-970-30
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-970-55) · 71205-970-55
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-970-60) · 71205-970-60
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-970-90) · 71205-970-90
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →