Constipation Relief
- Product NDC
- 17312-031
- Requested package NDC
- 17312-031-14
- 11-digit product format
- 173120031
- Labeler code
- 17312
- Product ID
- 17312-031_46051d5f-d0ec-e853-e063-6294a90a4922
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aloe, Potassium Alum, Oyster Shell Calcium Carbonate, Crude Activated Charcoal, Dioscorea Villosa Tuber, Veronicastrum Virginicum Root, Strychnos Nux Vomica Seed
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- TRP Company
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-04-15
- Substance
- ACTIVATED CHARCOAL; ALOE; DIOSCOREA VILLOSA ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; POTASSIUM ALUM; STRYCHNOS NUX-VOMICA SEED; VERONICASTRUM VIRGINICUM ROOT
- Active strength
- 6; 6; 6; 6; 6; 6; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- 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], Seed Storage Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2019-12-08 06:16 UTC · source 2019-12-05 | excluded package | package | 17312-031 | 17312-031-14 | E | Excluded after deficient or non-compliant submission was not corrected | excluded / ndc_excluded.zip | 110d247fa046… | a55b01930146… |
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Constipation Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| 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 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| IWY3IWX2G8 | Internal UNII lookup |
| 2P3VWU3H10 | Internal UNII lookup |
| 2E32821G6I | Internal UNII lookup |
| 1L24V9R23S | Internal UNII lookup |
| V5VD430YW9 | Internal UNII lookup |
| 269XH13919 | Internal UNII lookup |
| M2O62YTN42 | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 12dea1d1-9510-5aad-e054-00144ff8d46c | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| a62a50ac-1535-4461-9768-8ae703e2e9fb | Product name | 1 | 20210525 |
| 6084a4f4-5437-c9a5-caec-5361ee075a59 | Product name | 1 | 20140508 |
| 90c5639a-61b0-88d6-ddcf-21888e94869a | Product name | 1 | 20140508 |
| 9514609b-a2a9-f8ec-6ba6-3f8e5ee89877 | Product name | 1 | 20140508 |
| bc07ef78-e82d-0c19-31f4-31f263780582 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17312-031-14 | Constipation Relief | 1 in 1 PACKAGE | TABLET, ORALLY DISINTEGRATING | 1 | 5 | |
| 17312-031-14 | Constipation Relief | 50 in 1 BOTTLE | TABLET, ORALLY DISINTEGRATING | 50 | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17312-031 | CONSTIPATION RELIEF (ALOE, POTASSIUM ALUM, OYSTER SHELL CALCIUM CARBONATE, CRUDE ACTIVATED CHARCOAL, DIOSCOREA VILLOSA TUBER, VERONICASTRUM VIRGINICUM ROOT, STRYCHNOS NUX VOMICA SEED) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] | 4 | Current NDC, Legacy NDC, 2 package rows | 20230111_12dea1d1-9510-5aad-e054-00144ff8d46c.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Constipation Relief | ALOE, POTASSIUM ALUM, OYSTER SHELL CALCIUM CARBONATE, CRUDE ACTIVATED CHARCOAL, DIOSCOREA VILLOSA TUBER, VERONICASTRUM VIRGINICUM ROOT, STRYCHNOS NUX VOMICA SEED | TRP Company | 12dea1d1-9510-5aad-e054-00144ff8d46c | 2025-12-15 | Warnings | 17312-031-14 17312-031 17312003114 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 17312-031-14 | 17312003114 | 1 BOTTLE in 1 PACKAGE (17312-031-14) / 50 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE | 1 bottle | 2015-04-15 | 0000-00-00 | No | No | Current |