United States · FDA National Drug Code directory
Senokot-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
- 67618-310_e5dc8b86-705c-4b54-a9fe-20d02d62ad48
- Product NDC
- 67618-310
- Form
- TABLET
- Composition / generic term
- standardized senna concentrate and docusate sodium
- Labeler
- Atlantis Consumer Healthcare, Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 19741001
- Source listing expiry
- 20271231
Source-listed ingredients
- SENNOSIDES — 8.6 mg/1
- DOCUSATE SODIUM — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (67618-310-01) / 10 TABLET in 1 BLISTER PACK · 67618-310-01
- 1 BOTTLE, PLASTIC in 1 CARTON (67618-310-30) / 30 TABLET in 1 BOTTLE, PLASTIC · 67618-310-30
- 1 BOTTLE, PLASTIC in 1 CARTON (67618-310-60) / 60 TABLET in 1 BOTTLE, PLASTIC · 67618-310-60
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 →