United States · FDA National Drug Code directory
Constipation Relief
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
- 17312-031_46051d5f-d0ec-e853-e063-6294a90a4922
- Product NDC
- 17312-031
- Form
- TABLET, ORALLY DISINTEGRATING
- Composition / generic term
- Aloe, Potassium Alum, Oyster Shell Calcium Carbonate, Crude Activated Charcoal, Dioscorea Villosa Tuber, Veronicastrum Virginicum Root, Strychnos Nux Vomica Seed
- Labeler
- TRP Company
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20150415
- Source listing expiry
- 20261231
Source-listed ingredients
- DIOSCOREA VILLOSA ROOT — 6 [hp_X]/1
- ACTIVATED CHARCOAL — 6 [hp_X]/1
- OYSTER SHELL CALCIUM CARBONATE, CRUDE — 6 [hp_X]/1
- POTASSIUM ALUM — 6 [hp_X]/1
- ALOE — 6 [hp_X]/1
- STRYCHNOS NUX-VOMICA SEED — 6 [hp_X]/1
- VERONICASTRUM VIRGINICUM ROOT — 6 [hp_X]/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 PACKAGE (17312-031-14) / 50 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE · 17312-031-14
Source and coverage
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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.
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