What is NDC 17312-031?

17312-031 is the product NDC for Constipation Relief, Dioscorea villosa root 6 [hp_X]/1 + 6 more ingredients tablet, orally disintegrating, listed with the FDA by TRP Company. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Constipation Relief (Aloe, Potassium Alum, Oyster Shell Calcium Carbonate, Crude Activated Charcoal, Dioscorea Villosa Tuber, Veronicastrum Virginicum Root, Strychnos Nux Vomica Seed).

What is the active ingredient?

Dioscorea villosa root, Activated charcoal, Oyster shell calcium carbonate, Crude, Potassium alum, Aloe, Strychnos nux-vomica seed, Veronicastrum virginicum root.

TRP Company, NDC labeler code 17312. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Constipation Relief?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Constipation Relief NDC 17312-031 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17312-031Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17312-0031Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
17312-031-14	17312003114	1 BOTTLE in 1 PACKAGE (17312-031-14) / 50 TABLET, ORALLY DISINTEGRATING in 1 BOTTLEMarketed from Apr 15, 2015

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Constipation Relief
Generic name (nonproprietary): aloe, potassium alum, oyster shell calcium carbonate, crude activated charcoal, dioscorea villosa tuber, veronicastrum virginicum root, strychnos nux vomica seed
Active ingredients: Dioscorea villosa root — 6 [hp_X]/1Activated charcoal — 6 [hp_X]/1Oyster shell calcium carbonate, Crude — 6 [hp_X]/1Potassium alum — 6 [hp_X]/1Aloe — 6 [hp_X]/1Strychnos nux-vomica seed — 6 [hp_X]/1Veronicastrum virginicum root — 6 [hp_X]/1
Dosage form: Tablet, Orally disintegrating
Route: Oral
Labeler: TRP CompanyNDC labeler code 17312
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 15, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 17312-031_46051d5f-d0ec-e853-e063-6294a90a4922SPL ID 46051d5f-d0ec-e853-e063-6294a90a4922SPL set ID 12dea1d1-9510-5aad-e054-00144ff8d46cUNII IWY3IWX2G8, 2P3VWU3H10, 2E32821G6I, 1L24V9R23S, V5VD430YW9, 269XH13919, M2O62YTN42
Pharmacologic class: Non-Standardized Plant Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N417312003114 followed by a unit qualifier and the quantity

Package 17312-0031-14. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Dec 15, 2025.

Indications (excerpt from the label)

Uses:* According to homeopathic indications these ingredients temporarily relieve symptoms such as: • difficult elimination • dry, hard stools • cramping • ineffectual urgings and evacuation • gas • bloating • hemorrhoids. * These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17312-031

What is NDC 17312-031?: 17312-031 is the product NDC for Constipation Relief, Dioscorea villosa root 6 [hp_X]/1 + 6 more ingredients tablet, orally disintegrating, listed with the FDA by TRP Company. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Constipation Relief (Aloe, Potassium Alum, Oyster Shell Calcium Carbonate, Crude Activated Charcoal, Dioscorea Villosa Tuber, Veronicastrum Virginicum Root, Strychnos Nux Vomica Seed).
What is the active ingredient?: Dioscorea villosa root, Activated charcoal, Oyster shell calcium carbonate, Crude, Potassium alum, Aloe, Strychnos nux-vomica seed, Veronicastrum virginicum root.
Who is the labeler?: TRP Company, NDC labeler code 17312. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Constipation Relief?: 1 other product NDC are listed under this name. See all Constipation Relief NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Constipation Relief NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Constipation Reliefaluminum oxide, bryonia alba root, sodium chloride, graphite, silicon dioxide	Aluminum oxide 10 [hp_X]/4g + 4 more ingredients	PelletSublingual	Homeocare Laboratories	61727-304	61727-0304-21