United States · FDA National Drug Code directory

Gentle Laxative

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
50804-329_4a81b0be-b35d-4a3f-bb8b-4728ff30d2e4
Product NDC
50804-329
Form
TABLET, DELAYED RELEASE
Composition / generic term
Bisacodyl
Labeler
Geiss, Destin & Dunn Inc.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20260717
Source listing expiry
20271231

Source-listed ingredients

  • BISACODYL — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (50804-329-56) / 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 50804-329-56

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 →