What is NDC 44911-0495?

44911-0495 is the product NDC for Nerve Pro HP, Plantago major whole 6 [hp_X]/mL + 9 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Nerve Pro HP (Plantago Major, Xanthoxylum Fraxineum, Colocynthis, Magnesia Phosphorica, Agaricus Muscarius, Hypericum Perforatum, Argentum Nitricum, Carboneum Sulphuratum, Curare, Thallium Metallicum).

What is the active ingredient?

Plantago major whole, Zanthoxylum americanum bark, Citrullus colocynthis fruit pulp, Magnesium phosphate, Dibasic trihydrate, Amanita muscaria fruiting body, Hypericum perforatum whole, Silver nitrate, Carbon disulfide, Tubocurarine chloride, Thallium.

Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Nerve Pro HP?

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.

Nerve Pro HP NDC 44911-0495 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0495Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0495Add 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
44911-0495-1	4491104950144911049501	30 mL in 1 BOTTLE, DROPPER (44911-0495-1)Marketed from May 14, 2019

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): Nerve Pro HPSuffix: HP
Generic name (nonproprietary): plantago major, xanthoxylum fraxineum, colocynthis, magnesia phosphorica, agaricus muscarius, hypericum perforatum, argentum nitricum, carboneum sulphuratum, curare, thallium metallicum
Active ingredients: Plantago major whole — 6 [hp_X]/mLZanthoxylum americanum bark — 6 [hp_X]/mLCitrullus colocynthis fruit pulp — 12 [hp_X]/mLMagnesium phosphate, Dibasic trihydrate — 12 [hp_X]/mLAmanita muscaria fruiting body — 12 [hp_X]/mLHypericum perforatum whole — 12 [hp_X]/mLSilver nitrate — 30 [hp_X]/mLCarbon disulfide — 30 [hp_X]/mLTubocurarine chloride — 30 [hp_X]/mLThallium — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.NDC labeler code 44911
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 14, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 44911-0495_c98c29e3-90b3-4b1d-8a1d-83f9a70075c6SPL ID c98c29e3-90b3-4b1d-8a1d-83f9a70075c6SPL set ID 846d5805-6f82-4cb4-b64c-adba6d3004e7UNII W2469WNO6U, A4KL1HMZ7T, 23H32AOH17, HF539G9L3Q, DIF093I037, XK4IUX8MNB, 95IT3W8JZE, S54S8B99E8, 900961Z8VR, AD84R52XLFUPC 0363113700879
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative

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

N444911049501 followed by a unit qualifier and the quantity

Package 44911-0495-01. 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 29, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms of tingling, burning, and dumbness in the hands and feet.** **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)

About NDC 44911-0495

What is NDC 44911-0495?: 44911-0495 is the product NDC for Nerve Pro HP, Plantago major whole 6 [hp_X]/mL + 9 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Nerve Pro HP (Plantago Major, Xanthoxylum Fraxineum, Colocynthis, Magnesia Phosphorica, Agaricus Muscarius, Hypericum Perforatum, Argentum Nitricum, Carboneum Sulphuratum, Curare, Thallium Metallicum).
What is the active ingredient?: Plantago major whole, Zanthoxylum americanum bark, Citrullus colocynthis fruit pulp, Magnesium phosphate, Dibasic trihydrate, Amanita muscaria fruiting body, Hypericum perforatum whole, Silver nitrate, Carbon disulfide, Tubocurarine chloride, Thallium.
Who is the labeler?: Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nerve Pro HP?: 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.