Nux Vomica NDC 15631-0317

NDC codes

FDA NDC Directory

Product NDC (as listed)15631-0317Labeler and product segments. Claims need a package NDC.

Product NDC at billing width15631-0317Add 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
15631-0317-0	15631031700	100 PELLET in 1 PACKAGE (15631-0317-0)Marketed from Jan 1, 2018
15631-0317-1	15631031701	200 PELLET in 1 PACKAGE (15631-0317-1)Marketed from Jan 1, 2018
15631-0317-2	15631031702	400 PELLET in 1 PACKAGE (15631-0317-2)Marketed from Jan 1, 2018
15631-0317-3	15631031703	750 PELLET in 1 PACKAGE (15631-0317-3)Marketed from Jan 1, 2018
15631-0317-4	15631031704	2500 PELLET in 1 PACKAGE (15631-0317-4)Marketed from Jan 1, 2018
15631-0317-5	15631031705	12500 PELLET in 1 PACKAGE (15631-0317-5)Marketed from Jan 1, 2018
15631-0317-6	15631031706	500 PELLET in 1 PACKAGE (15631-0317-6)Marketed from Aug 23, 2021
15631-0317-7	15631031707	1000 PELLET in 1 PACKAGE (15631-0317-7)Marketed from Aug 23, 2021

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Nux Vomica
Generic name (nonproprietary): nux vomica
Active ingredients: Strychnos nux-vomica seed — 3 [hp_X]/1
Dosage form: Pellet
Route: Oral
Labeler: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 10, 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 15631-0317_ca3b21cc-74c3-7a65-e053-2a95a90ae7c0SPL ID ca3b21cc-74c3-7a65-e053-2a95a90ae7c0SPL set ID 98af289f-969f-494d-8998-a5eea1c9e67eUNII 269XH13919UPC 8907460005526
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

N415631031700 followed by a unit qualifier and the quantity

Package 15631-0317-00. 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 Aug 23, 2021.

Indications (excerpt from the label)

INDICATIONS Condition listed above or as directed by the physician

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)