What is NDC 71781-0001?

71781-0001 is the product NDC for Homeoplex A, American ginseng 3 [hp_X]/mL + 9 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 A (Aralia Quinquefolia, Avena Sativa, Glandula Suprarenalis Suis, Arsenicum Iodatum, Ignatia Amara, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Zincum Metallicum).

What is the active ingredient?

American ginseng, Avena sativa flowering top, Sus scrofa adrenal gland, Arsenic triiodide, Strychnos ignatii seed, Lycopodium clavatum spore, Strychnos nux-vomica seed, Phosphoric acid, Phosphorus, Zinc.

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 A?

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.

Homeoplex A NDC 71781-0001 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71781-0001Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71781-0001Add 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
71781-0001-1	7178100010171781000101	60 mL in 1 BOTTLE, DROPPER (71781-0001-1)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 A
Generic name (nonproprietary): aralia quinquefolia, avena sativa, glandula suprarenalis suis, arsenicum iodatum, ignatia amara, lycopodium clavatum, nux vomica, phosphoricum acidum, phosphorus, zincum metallicum
Active ingredients: American ginseng — 3 [hp_X]/mLAvena sativa flowering top — 3 [hp_X]/mLSus scrofa adrenal gland — 6 [hp_X]/mLArsenic triiodide — 12 [hp_X]/mLStrychnos ignatii seed — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLZinc — 12 [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: Oct 31, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 71781-0001_abc6ac3d-e222-4c98-a9cf-1b6dbce52f4aSPL ID abc6ac3d-e222-4c98-a9cf-1b6dbce52f4aSPL set ID fee279bf-76b7-4a84-ac8c-cd2489a910fbUNII 8W75VCV53Q, MA9CQJ3F7F, 398IYQ16YV, 3029988O2T, 1NM3M2487K, C88X29Y479, 269XH13919, E4GA8884NN, 27YLU75U4W, J41CSQ7QDSUPC 0799861441168
Pharmacologic class: Non-Standardized Plant Allergenic Extract

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

N471781000101 followed by a unit qualifier and the quantity

Package 71781-0001-01. 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 Nov 1, 2017.

Indications (excerpt from the label)

INDICATIONS: For support of adrenal system.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71781-0001

What is NDC 71781-0001?: 71781-0001 is the product NDC for Homeoplex A, American ginseng 3 [hp_X]/mL + 9 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 A (Aralia Quinquefolia, Avena Sativa, Glandula Suprarenalis Suis, Arsenicum Iodatum, Ignatia Amara, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Zincum Metallicum).
What is the active ingredient?: American ginseng, Avena sativa flowering top, Sus scrofa adrenal gland, Arsenic triiodide, Strychnos ignatii seed, Lycopodium clavatum spore, Strychnos nux-vomica seed, Phosphoric acid, Phosphorus, Zinc.
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 A?: 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.