Metex 6013 (metex) NDC 63083-6013

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-6013Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-6013Add 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
63083-6013-2	63083601302	59 mL in 1 BOTTLE, DROPPER (63083-6013-2)Marketed from Aug 15, 1985

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): Metex 6013Suffix: 6013
Generic name (nonproprietary): metex
Active ingredients: Plantago major whole — 3 [hp_X]/59mLCopper — 6 [hp_X]/59mLLycopodium clavatum spore — 6 [hp_X]/59mLAluminum oxide — 30 [hp_X]/59mLArsenic trioxide — 30 [hp_X]/59mLCadmium — 30 [hp_X]/59mLMercurius solubilis — 30 [hp_X]/59mLNickel sulfate hexahydrate — 30 [hp_X]/59mLLead — 30 [hp_X]/59mLRubidium — 30 [hp_X]/59mLStainless steel 316l — 30 [hp_X]/59mLTitanium — 30 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 63083-6013_0d802602-9503-40a2-8191-c6d08c514b00SPL ID 0d802602-9503-40a2-8191-c6d08c514b00SPL set ID 78371ca3-50a6-46f0-8ea6-7de57c516375UNII W2469WNO6U, 789U1901C5, C88X29Y479, LMI26O6933, S7V92P67HO, 00BH33GNGH, 324Y4038G2, JC9WZ4FK68, 2P299V784P, MLT4718TJW, F0T1G9Y758, D1JT611TNE
Pharmacologic class: Copper-containing Intrauterine Device

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

N463083601302 followed by a unit qualifier and the quantity

Package 63083-6013-02. 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 Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of occasional headache, weakness or tiredness, minor joint or muscle aches, constipation, nausea or vomiting, or confusion due to sensitivity to or exposure to heavy metals.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)