Vermasode NDC 43406-0679

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0679Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0679Add 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
43406-0679-1	43406067901	30 mL in 1 BOTTLE, DROPPER (43406-0679-1)Marketed from Jun 13, 2018

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): Vermasode
Generic name (nonproprietary): artemisia vulgaris, chelidonium majus, granatum, spigelia anthelmia, ratanhia, arsenicum album, ferrum metallicum, calcarea carbonica, cina, gaertner bacillus, graphites, mercurius dulcis, natrum muriaticum, natrum phosphoricum, vermin nosode
Active ingredients: Artemisia vulgaris root — 4 [hp_X]/mLChelidonium majus whole — 4 [hp_X]/mLPunica granatum root bark — 4 [hp_X]/mLSpigelia anthelmia whole — 4 [hp_X]/mLKrameria lappacea root — 4 [hp_X]/mLArsenic trioxide — 6 [hp_X]/mLIron — 9 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLArtemisia cina pre-flowering top — 12 [hp_X]/mLSalmonella enterica enterica serovar enteritidis — 12 [hp_X]/mLGraphite — 12 [hp_X]/mLCalomel — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLSodium phosphate, Dibasic, Heptahydrate — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Natural Creations, Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 13, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 43406-0679_f1d2ebf6-713d-49e0-a01e-c17877c586e2SPL ID f1d2ebf6-713d-49e0-a01e-c17877c586e2SPL set ID 180b5641-5692-42d4-8472-fdadccebd746UNII 32MP823R8S, 7E889U5RNN, CLV24I3T1D, WYT05213GE, P29ZH1A35Z, S7V92P67HO, E1UOL152H7, 2E32821G6I, 28M1820ACT, Y3V16D4PV4, 4QQN74LH4O, J2D46N657D, 451W47IQ8X, 70WT22SF4BUPC 0877730003065

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

N443406067901 followed by a unit qualifier and the quantity

Package 43406-0679-01. 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 18, 2025.

Indications (excerpt from the label)

USES: Temporarily relieves symptoms caused by pinworm infestation.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)