Over-the-counter drug · UNAPPROVED HOMEOPATHIC
D-6 NDC 58264-0006
Aconitum napellus 4 [hp_X]/mL + 9 more ingredients · Solution · Sublingual · DNA Labs, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 58264-0006-1 | 58264000601 | 29.57 mL in 1 BOTTLE, GLASS (58264-0006-1)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)
- D-6
- Generic name (nonproprietary)
- aconitum napellus, bryonia alba whole, eupatorium perfoliatum flowering top, gelsemium sempervirens root, causticum, camphor (natural), eucalyptus globulus leaf, baptisia tinctoria, ferrosoferric phosphate, and schoenocaulon officinale seed
- Active ingredients
- Aconitum napellus — 4 [hp_X]/mLBryonia alba whole — 4 [hp_X]/mLEupatorium perfoliatum flowering top — 3 [hp_X]/mLGelsemium sempervirens root — 6 [hp_X]/mLCausticum — 6 [hp_X]/mLCamphor (Natural) — 3 [hp_X]/mLEucalyptus globulus leaf — 3 [hp_X]/mLBaptisia tinctoria — 4 [hp_X]/mLFerrosoferric phosphate — 8 [hp_X]/mLSchoenocaulon officinale seed — 6 [hp_X]/mL
- Dosage form
- Solution
- Route
- Sublingual
- Labeler
- DNA Labs, Inc.
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 58264-0006_2b9ea383-d6c5-326c-e063-6394a90ace3dSPL ID 2b9ea383-d6c5-326c-e063-6394a90ace3dSPL set ID 27f58993-c611-4dc7-ac8e-0132f0a4fcefUNII U0NQ8555JD, 56K0VVT47P, 1W0775VX6E, 639KR60Q1Q, DD5FO1WKFU, N20HL7Q941, S546YLW6E6, 5K1UO2888Y, 91GQH8I5F7, 6NAF1689IO
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
N458264000601followed by a unit qualifier and the quantityPackage 58264-0006-01. 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 Dull headaches, restlessness, feverish, aches all over the body.
Excerpt only. Read the full label for complete information.