Thiosinaminum (allylthiourea) NDC 0220-4971

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-4971Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-4971Add 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
0220-4971-41	00220497141	30 [hp_C] in 1 TUBE (0220-4971-41)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): Thiosinaminum
Generic name (nonproprietary): allylthiourea
Active ingredients: Allylthiourea — 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
Identifiers: Product ID 0220-4971_f2f5c1ee-8932-321c-e053-2995a90a2717SPL ID f2f5c1ee-8932-321c-e053-2995a90a2717SPL set ID 86590806-9e23-d0f5-e053-2991aa0a14eaUNII 706IDJ14B7

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

N400220497141 followed by a unit qualifier and the quantity

Package 00220-4971-41. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.