Met Tox NDC 73421-0526

NDC codes

FDA NDC Directory

Product NDC (as listed)73421-0526Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73421-0526Add 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
73421-0526-1	73421052601	29.6 mL in 1 BOTTLE, DROPPER (73421-0526-1)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): Met Tox
Generic name (nonproprietary): arsenicum alb, avena, berberis vulg, lycopodium, nat mur, nux vom, phytolacca, rhamnus frang, solidago, trifolium prat
Active ingredients: Arsenic trioxide — 12 [hp_X]/29.6mLAvena sativa flowering top — 3 [hp_X]/29.6mLBerberis vulgaris root bark — 3 [hp_X]/29.6mLLycopodium clavatum spore — 12 [hp_X]/29.6mLSodium chloride — 12 [hp_X]/29.6mLStrychnos nux-vomica seed — 12 [hp_X]/29.6mLPhytolacca americana root — 3 [hp_X]/29.6mLFrangula alnus bark — 3 [hp_X]/29.6mLSolidago virgaurea flowering top — 3 [hp_X]/29.6mLTrifolium pratense flower — 3 [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 73421-0526_eedfd248-253f-2c60-e053-2a95a90a44f1SPL ID eedfd248-253f-2c60-e053-2a95a90a44f1SPL set ID 2653d62b-5dd7-482c-b31c-ce5fa1373900UNII S7V92P67HO, MA9CQJ3F7F, 1TH8Q20J0U, C88X29Y479, 451W47IQ8X, 269XH13919, 11E6VI8VEG, S2D77IH61R, 5405K23S50, 4JS0838828
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

N473421052601 followed by a unit qualifier and the quantity

Package 73421-0526-01. 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 exhaustion, weakness, aching, soreness and restlessness. (**)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)