Homeoplex B NDC 71781-0002

NDC codes

FDA NDC Directory

Product NDC (as listed)71781-0002Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71781-0002Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
71781-0002-1	71781000201	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.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 31, 2017
Listing expires: Dec 31, 2026
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

N471781000201 followed by a unit qualifier and the quantity

Package 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 Oct 31, 2017.

Indications (excerpt from the label)

INDICATIONS: For support of neuroaffect function.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)