Mycocan 30X 4042 (mycocan 30x) NDC 63083-4042

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-4042Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-4042Add 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
63083-4042-2	63083404202	59 mL in 1 BOTTLE, DROPPER (63083-4042-2)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): Mycocan 30X 4042Suffix: 4042
Generic name (nonproprietary): mycocan 30x
Active ingredients: Candida albicans — 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: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 63083-4042_dd432641-b2c0-411f-9e2c-ec98969a0f1cSPL ID dd432641-b2c0-411f-9e2c-ec98969a0f1cSPL set ID 76faf3a2-af82-42b3-8056-0d8ba0446c8cUNII 4D7G21HDBC
Pharmacologic class: Non-Standardized Fungal 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

N463083404202 followed by a unit qualifier and the quantity

Package 63083-4042-02. 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 fatigue, bloating, constipation or diarrhea, difficulty concentrating or lack of focus, minor skin rash, irritability, seasonal allergies, or sugar or carbohydrate cravings.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)