Over-the-counter drug · UNAPPROVED HOMEOPATHIC
D-39 NDC 58264-0039
Lachesis muta venom 30 [hp_X]/mL + 4 more ingredients · Solution · Sublingual · DNA Labs, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 58264-0039-1 | 58264003901 | 29.57 mL in 1 BOTTLE, GLASS (58264-0039-1)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-39
- Generic name (nonproprietary)
- lachesis muta venom, lycopodium clavatum spore, palladium, saxifraga granulata whole, and vespa crabro
- Active ingredients
- Lachesis muta venom — 30 [hp_X]/mLLycopodium clavatum spore — 30 [hp_X]/mLPalladium — 12 [hp_X]/mLSaxifraga granulata whole — 30 [hp_X]/mLVespa crabro — 12 [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 58264-0039_2b9ecbda-7107-d64a-e063-6294a90aac9eSPL ID 2b9ecbda-7107-d64a-e063-6294a90aac9eSPL set ID 0d997878-b973-45aa-a319-9194fcecc5fcUNII VSW71SS07I, C88X29Y479, 5TWQ1V240M, W1LUS9R48G, K3ALM8S49H
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
N458264003901followed by a unit qualifier and the quantityPackage 58264-0039-01. 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 Supports ovary on the left side.
Excerpt only. Read the full label for complete information.
About NDC 58264-0039
- What is NDC 58264-0039?
- 58264-0039 is the product NDC for D-39, Lachesis muta venom 30 [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?
- D-39 (LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, PALLADIUM, SAXIFRAGA GRANULATA WHOLE, and Vespa crabro).
- What is the active ingredient?
- Lachesis muta venom, Lycopodium clavatum spore, Palladium, Saxifraga granulata whole, Vespa crabro.
- 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 D-39?
- 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.