Kreosotum (wood creosote) NDC 0220-2940

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-2940Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-2940Add 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
0220-2940-41	00220294041	1 [hp_M] in 1 TUBE (0220-2940-41)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): Kreosotum
Generic name (nonproprietary): wood creosote
Active ingredients: Wood creosote — 1 [hp_M]/[hp_M]
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 0220-2940_0a0e390d-fe5e-9dc6-e063-6294a90a5f58SPL ID 0a0e390d-fe5e-9dc6-e063-6294a90a5f58SPL set ID 8619e4e5-0c55-45db-e053-2a91aa0aa6b7UNII 3JYG22FD73

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

N400220294041 followed by a unit qualifier and the quantity

Package 00220-2940-41. 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.