Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Formica rufa NDC 0220-2139
Formica rufa 30 [hp_C]/30[hp_C] · Pellet · Oral · Boiron
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0220-2139-41 | 00220213941 | 30 [hp_C] in 1 TUBE (0220-2139-41)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)
- Formica rufa
- Generic name (nonproprietary)
- formica rufa
- Active ingredients
- Formica rufa — 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
- Listing expires
- Identifiers
- Product ID 0220-2139_f19eb662-8f05-69f9-e053-2a95a90a7939SPL ID f19eb662-8f05-69f9-e053-2a95a90a7939SPL set ID 87377727-5cb1-23cc-e053-2a91aa0a9413UNII 55H0W83JO5
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
N400220213941followed by a unit qualifier and the quantityPackage 00220-2139-41. 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 .
Indications (excerpt from the label)
Joint pains*
Excerpt only. Read the full label for complete information.