Mytox 6021 (mytox) NDC 63083-6021

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-6021Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-6021Add 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
63083-6021-2	63083602102	59 mL in 1 BOTTLE, DROPPER (63083-6021-2)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): Mytox 6021Suffix: 6021
Generic name (nonproprietary): mytox
Active ingredients: Sodium borate — 4 [hp_X]/59mLColchicum autumnale bulb — 4 [hp_X]/59mLAmanita muscaria fruiting body — 6 [hp_X]/59mLArsenic trioxide — 6 [hp_X]/59mLDrosera rotundifolia whole — 6 [hp_X]/59mLBufo bufo cutaneous gland — 8 [hp_X]/59mLUbidecarenone — 12 [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
Identifiers: Product ID 63083-6021_f48bbd72-9f6f-4aa4-8777-d02e3830d7c6SPL ID f48bbd72-9f6f-4aa4-8777-d02e3830d7c6SPL set ID bc89020f-c089-4351-a700-0ed19ec81604UNII 91MBZ8H3QO, 993QHL78E6, DIF093I037, S7V92P67HO, QR44N9XPJQ, Q59QU6N72Q, EJ27X76M46

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

N463083602102 followed by a unit qualifier and the quantity

Package 63083-6021-02. 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 red or itchy skin, cough, joint or muscle pain or stiffness, shortness of breath, sneezing, occasional headache, dizziness, or fatigue.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)