Over-the-counter drug · UNAPPROVED HOMEOPATHIC
N-19 NDC 58264-0217
Formica rufa 12 [hp_X]/mL + 4 more ingredients · Solution · Sublingual · DNA Labs, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 58264-0217-1 | 5826402170158264021701 | 29.57 mL in 1 BOTTLE, GLASS (58264-0217-1)Marketed from Jan 1, 1990 |
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)
- N-19
- Generic name (nonproprietary)
- formica rufa, potassium carbonate, kalmia latifolia whole, zanthoxylum americanum bark, and bos taurus parathyroid gland
- Active ingredients
- Formica rufa — 12 [hp_X]/mLPotassium carbonate — 6 [hp_X]/mLKalmia latifolia whole — 6 [hp_X]/mLZanthoxylum americanum bark — 6 [hp_X]/mLBos taurus parathyroid gland — 200 [hp_X]/mL
- Dosage form
- Solution
- Route
- Sublingual
- Labeler
- DNA Labs, Inc.NDC labeler code 58264
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 58264-0217_2b539a4e-f4ab-fd07-e063-6294a90a32b9SPL ID 2b539a4e-f4ab-fd07-e063-6294a90a32b9SPL set ID 1ceb1572-1e45-4c35-a075-b569478156c0UNII 55H0W83JO5, BQN1B9B9HA, P1SWF7DK1Y, A4KL1HMZ7T, SMV71DDI4T
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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N458264021701followed by a unit qualifier and the quantityPackage 58264-0217-01. 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)
INDICATIONS Support for the Parathyroid.
Excerpt only. Read the full label for complete information.
About NDC 58264-0217
- What is NDC 58264-0217?
- 58264-0217 is the product NDC for N-19, Formica rufa 12 [hp_X]/mL + 4 more ingredients solution, listed with the FDA by DNA Labs, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- N-19 (Formica rufa, POTASSIUM CARBONATE, KALMIA LATIFOLIA WHOLE, ZANTHOXYLUM AMERICANUM BARK, and BOS TAURUS PARATHYROID GLAND).
- What is the active ingredient?
- Formica rufa, Potassium carbonate, Kalmia latifolia whole, Zanthoxylum americanum bark, Bos taurus parathyroid gland.
- Who is the labeler?
- DNA Labs, Inc., NDC labeler code 58264. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for N-19?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.