V HP NDC 44911-0680

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0680Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0680Add 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
44911-0680-1	44911068001	60 mL in 1 BOTTLE, DROPPER (44911-0680-1)Marketed from Aug 23, 2023

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): V HPSuffix: HP
Generic name (nonproprietary): anas barbariae, hepatis et cordis extractum, arsenicum album, belladonna, bryonia (alba), carcinosin, echinacea (angustifolia), eupatorium perfoliatum, gelsemium sempervirens, lycopodium clavatum, natrum muriaticum, phosphoricum acidum, phosphorus, pyrogenium, rhus tox, sulphur
Active ingredients: Cairina moschata heart/liver autolysate — 30 [hp_X]/mLArsenic trioxide — 30 [hp_X]/mLAtropa belladonna — 30 [hp_X]/mLBryonia alba root — 30 [hp_X]/mLHuman breast tumor cell — 30 [hp_X]/mLEchinacea angustifolia whole — 30 [hp_X]/mLEupatorium perfoliatum flowering top — 30 [hp_X]/mLGelsemium sempervirens root — 30 [hp_X]/mLLycopodium clavatum spore — 30 [hp_X]/mLSodium chloride — 30 [hp_X]/mLPhosphoric acid — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLRancid beef — 30 [hp_X]/mLToxicodendron pubescens leaf — 30 [hp_X]/mLSulfur — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 23, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0680_1a9b2343-08a2-4d58-a9fe-78fe2af3fbf3SPL ID 1a9b2343-08a2-4d58-a9fe-78fe2af3fbf3SPL set ID cba32ae8-45af-494c-ac1a-fea4b10f1860UNII RN2HC612GY, S7V92P67HO, WQZ3G9PF0H, T7J046YI2B, C62OO7VD9K, VB06AV5US8, 1W0775VX6E, 639KR60Q1Q, C88X29Y479, 451W47IQ8X, E4GA8884NN, 27YLU75U4W, 29SUH5R3HU, 6IO182RP7A, 70FD1KFU70UPC 0363113700985

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

N444911068001 followed by a unit qualifier and the quantity

Package 44911-0680-01. 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 Dec 4, 2025.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms due to poor immune function, such as chronic fatigue, headache, and sore throat.** **Claims based on traditional homeopathic practice, not accepted medical evidence Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)