Nux Vomica (strychnos nux-vomica seed) NDC 0220-3681

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-3681Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-3681Add 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
0220-3681-41	00220368141	80 PELLET in 1 TUBE (0220-3681-41)Marketed from Jan 1, 2012
0220-3681-43	00220368143	3 TUBE in 1 PACKAGE (0220-3681-43) / 80 PELLET in 1 TUBE (0220-3681-41)Marketed from Jan 1, 2012

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Nux Vomica
Generic name (nonproprietary): strychnos nux-vomica seed
Active ingredients: Strychnos nux-vomica seed — 30 [hp_C]/1
Dosage form: Pellet
Route: Oral
Labeler: Laboratoires Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2012
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 0220-3681_19113686-5d82-2c3f-e063-6294a90afd32SPL ID 19113686-5d82-2c3f-e063-6294a90afd32SPL set ID d1db2f1c-fe9d-47de-a77d-ffb291297751UNII 269XH13919UPC 0000200007311
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

N400220368141 followed by a unit qualifier and the quantity

Package 00220-3681-41. 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 May 22, 2024.

Indications (excerpt from the label)

Hangover Relief Uses* temporarily relieves upset stomach associated with nausea or fullness due to overindulgence in drink or food temporarily relieves occasional heartburn, acid indigestion, or sour stomach temporarily relieves irritability due to hypersensitivity to light, noise, odor or touch Indigestion Relief Uses* temporarily relieves upset stomach associated with nausea or fullness due to overindulgence in drink or food temporarily relieves occasional heartburn, acid indigestion, or sour stomach Tube Uses* Relieves heartburn or drowsiness due to excessive eating or drinking, Irritability *

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)