Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Homeoplex B NDC 71781-0002
Arsenic trioxide 30 [hp_X]/mL + 8 more ingredients · Liquid · Oral · Supplement Clinic, LLC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71781-0002-1 | 7178100020171781000201 | 60 mL in 1 BOTTLE, DROPPER (71781-0002-1)Marketed from Oct 31, 2017 |
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)
- Homeoplex B
- Generic name (nonproprietary)
- arsenicum album, calcarea carbonica , ignatia amara, kali carbonicum, lachesis mutus, natrum muriaticum, phosphorus, pulsatilla, staphysagria
- Active ingredients
- Arsenic trioxide — 30 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLStrychnos ignatii seed — 30 [hp_X]/mLPotassium carbonate — 30 [hp_X]/mLLachesis muta venom — 30 [hp_X]/mLSodium chloride — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLPulsatilla vulgaris — 30 [hp_X]/mLDelphinium staphisagria seed — 30 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Supplement Clinic, LLC.NDC labeler code 71781
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 71781-0002_9f23592b-5e83-47ee-b2b5-b2b255938bc1SPL ID 9f23592b-5e83-47ee-b2b5-b2b255938bc1SPL set ID e9a9c58e-1b70-4ac8-9d9c-108c628d7664UNII S7V92P67HO, 2E32821G6I, 1NM3M2487K, BQN1B9B9HA, VSW71SS07I, 451W47IQ8X, 27YLU75U4W, I76KB35JEV, 00543AP1JVUPC 0799861441175
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
N471781000201followed by a unit qualifier and the quantityPackage 71781-0002-01. 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: For support of neuroaffect function.
Excerpt only. Read the full label for complete information.
About NDC 71781-0002
- What is NDC 71781-0002?
- 71781-0002 is the product NDC for Homeoplex B, Arsenic trioxide 30 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Supplement Clinic, LLC.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Homeoplex B (Arsenicum Album, Calcarea Carbonica , Ignatia Amara, Kali Carbonicum, Lachesis Mutus, Natrum Muriaticum, Phosphorus, Pulsatilla, Staphysagria).
- What is the active ingredient?
- Arsenic trioxide, Oyster shell calcium carbonate, Crude, Strychnos ignatii seed, Potassium carbonate, Lachesis muta venom, Sodium chloride, Phosphorus, Pulsatilla vulgaris, Delphinium staphisagria seed.
- Who is the labeler?
- Supplement Clinic, LLC., NDC labeler code 71781. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Homeoplex B?
- 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.