Virex NDC 73421-1027

NDC codes

FDA NDC Directory

Product NDC (as listed)73421-1027Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73421-1027Add 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
73421-1027-1	73421102701	29.6 mL in 1 BOTTLE (73421-1027-1)Marketed from Jun 1, 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): Virex
Generic name (nonproprietary): arsenicum alb, baptisia, belladonna, echinacea, eupatorium perf, gelsemium, lycopodium, , nux vom, phosphoricum ac, phosphorus, pyrogenium, rhus tox
Active ingredients: Arsenic trioxide — 12 [hp_X]/29.6mLBaptisia tinctoria root — 3 [hp_X]/29.6mLAtropa belladonna — 12 [hp_X]/29.6mLEchinacea angustifolia whole — 3 [hp_X]/29.6mLEupatorium perfoliatum flowering top — 12 [hp_X]/29.6mLGelsemium sempervirens root — 12 [hp_X]/29.6mLLycopodium clavatum spore — 12 [hp_X]/29.6mLStrychnos nux-vomica seed — 12 [hp_X]/29.6mLPhosphoric acid — 12 [hp_X]/29.6mLPhosphorus — 12 [hp_X]/29.6mLRancid beef — 30 [hp_X]/29.6mLToxicodendron pubescens leaf — 30 [hp_X]/29.6mL
Dosage form: Liquid
Route: Oral
Labeler: White Manufacturing Inc. DBA Micro-West
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 1, 2021
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 73421-1027_eedfd248-255d-2c60-e053-2a95a90a44f1SPL ID eedfd248-255d-2c60-e053-2a95a90a44f1SPL set ID 77b9e94e-e159-4b77-bd8a-9f5937ac2906UNII S7V92P67HO, 5EF0HWI5WU, WQZ3G9PF0H, VB06AV5US8, 1W0775VX6E, 639KR60Q1Q, C88X29Y479, 269XH13919, E4GA8884NN, 27YLU75U4W, 29SUH5R3HU, 6IO182RP7A
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

N473421102701 followed by a unit qualifier and the quantity

Package 73421-1027-01. 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 2, 2022.

Indications (excerpt from the label)

INDICATIONS: For the temporary relief of heaviness, weakness, weariness, numbness, tingling, muscle soreness or aching. (**)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)