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 NDC11-digit (billing)PackageCopy
71781-0002-1717810002017178100020160 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

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 .

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)

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.

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