Ustilago Maidis (ustilago maydis) NDC 0220-5153

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-5153Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-5153Add 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
0220-5153-41	00220515341	30 [hp_C] in 1 TUBE (0220-5153-41)Marketed from Mar 3, 1983

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Ustilago Maidis
Generic name (nonproprietary): ustilago maydis
Active ingredients: Ustilago maydis — 30 [hp_C]/30[hp_C]
Dosage form: Pellet
Route: Oral
Labeler: Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 3, 1983
Listing expires: Dec 31, 2026
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 0220-5153_1e6649ad-2fa6-6737-e063-6394a90a7857SPL ID 1e6649ad-2fa6-6737-e063-6394a90a7857SPL set ID 861b3c1d-3b13-6ea6-e053-2991aa0ab4dcUNII 4K7Z7K7SWG
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

N400220515341 followed by a unit qualifier and the quantity

Package 00220-5153-41. 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 Jul 29, 2024.

Indications (excerpt from the label)

Uses: See symptoms on front panel. Relieves heavy menstruation *

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)