NDC product
Constipation Relief
NDC 17312-031 · TRP Company
Key facts
| Product NDC | 17312-031 |
|---|---|
| Proprietary name | Constipation Relief |
| Nonproprietary name | Aloe, Potassium Alum, Oyster Shell Calcium Carbonate, Crude Activated Charcoal, Dioscorea Villosa Tuber, Veronicastrum Virginicum Root, Strychnos Nux Vomica Seed |
| Substances | DIOSCOREA VILLOSA ROOT, ACTIVATED CHARCOAL, OYSTER SHELL CALCIUM CARBONATE, CRUDE, POTASSIUM ALUM, ALOE, STRYCHNOS NUX-VOMICA SEED, VERONICASTRUM VIRGINICUM ROOT |
| Dosage form | TABLET, ORALLY DISINTEGRATING |
| Route | ORAL |
| Labeler | TRP Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] and 1 more |
| Marketing start | Apr 15, 2015 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: