Over-the-counter drug · UNAPPROVED HOMEOPATHIC
D-10 NDC 58264-0010
Sepia officinalis whole 4 [hp_X]/mL + 4 more ingredients · Solution · Sublingual · DNA Labs, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 58264-0010-1 | 5826400100158264001001 | 29.57 mL in 1 BOTTLE, GLASS (58264-0010-1)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-10
- Generic name (nonproprietary)
- sepia officinalis whole, sanguinaria canadensis root, sulfuric acid, black cohosh, and lachesis muta venom
- Active ingredients
- Sepia officinalis whole — 4 [hp_X]/mLSanguinaria canadensis root — 4 [hp_X]/mLSulfuric acid — 4 [hp_X]/mLBlack cohosh — 4 [hp_X]/mLLachesis muta venom — 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 58264-0010_2b9ea65c-9dfb-ad89-e063-6394a90ab44cSPL ID 2b9ea65c-9dfb-ad89-e063-6394a90ab44cSPL set ID 1e5ba502-eef4-4df0-8330-b70d1872b4bbUNII 48GD5780QF, N9288CD508, O40UQP6WCF, K73E24S6X9, VSW71SS07I
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
N458264001001followed by a unit qualifier and the quantityPackage 58264-0010-01. 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 Flushes of heat.
Excerpt only. Read the full label for complete information.
About NDC 58264-0010
- What is NDC 58264-0010?
- 58264-0010 is the product NDC for D-10, Sepia officinalis whole 4 [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-10 (Sepia officinalis whole, Sanguinaria canadensis root, Sulfuric acid, Black cohosh, and Lachesis muta venom).
- What is the active ingredient?
- Sepia officinalis whole, Sanguinaria canadensis root, Sulfuric acid, Black cohosh, Lachesis muta venom.
- 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-10?
- 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.