What is NDC 71781-0006?

71781-0006 is the product NDC for Homeoplex L, Beta vulgaris 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 L (Beta Vulgaris, Carduus Marianus, Taraxacum Officinale, Cholesterinum, Fel Tauri, Chelidonium Majus, Lycopodium Clavatum, Natrum Sulphuricum, Nux Vomica, Phosphorus).

What is the active ingredient?

Beta vulgaris, Milk thistle, Taraxacum officinale, Cholesterol, Bos taurus bile, Chelidonium majus, Lycopodium clavatum spore, Sodium sulfate, Strychnos nux-vomica seed, Phosphorus.

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 L?

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 L NDC 71781-0006 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71781-0006Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71781-0006Add 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
71781-0006-1	7178100060171781000601	60 mL in 1 BOTTLE, DROPPER (71781-0006-1)Marketed from Nov 1, 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 L
Generic name (nonproprietary): beta vulgaris, carduus marianus, taraxacum officinale, cholesterinum, fel tauri, chelidonium majus, lycopodium clavatum, natrum sulphuricum, nux vomica, phosphorus
Active ingredients: Beta vulgaris — 3 [hp_X]/mLMilk thistle — 3 [hp_X]/mLTaraxacum officinale — 3 [hp_X]/mLCholesterol — 6 [hp_X]/mLBos taurus bile — 6 [hp_X]/mLChelidonium majus — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLSodium sulfate — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPhosphorus — 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: Nov 1, 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 71781-0006_d33b08fa-aa3b-445d-bd7b-02509835bbecSPL ID d33b08fa-aa3b-445d-bd7b-02509835bbecSPL set ID eefb2285-6d36-4c00-8054-44637f67d072UNII 4G174V5051, U946SH95EE, 39981FM375, 97C5T2UQ7J, ET3651ZLOU, 7E889U5RNN, C88X29Y479, 0YPR65R21J, 269XH13919, 27YLU75U4WUPC 0799861441199
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

N471781000601 followed by a unit qualifier and the quantity

Package 71781-0006-01. 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 general liver support.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71781-0006

What is NDC 71781-0006?: 71781-0006 is the product NDC for Homeoplex L, Beta vulgaris 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 L (Beta Vulgaris, Carduus Marianus, Taraxacum Officinale, Cholesterinum, Fel Tauri, Chelidonium Majus, Lycopodium Clavatum, Natrum Sulphuricum, Nux Vomica, Phosphorus).
What is the active ingredient?: Beta vulgaris, Milk thistle, Taraxacum officinale, Cholesterol, Bos taurus bile, Chelidonium majus, Lycopodium clavatum spore, Sodium sulfate, Strychnos nux-vomica seed, Phosphorus.
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 L?: 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.