What is NDC 44911-0625?

44911-0625 is the product NDC for Numbness HP, Aconitum napellus whole 30 [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?

Numbness HP (Aconitum napellus, Agaricus muscarius, Allium cepa, Arnica montana, Coffea cruda, Hypericum perforatum, Lycopodium clavatum, Mercurius solubilis, Phosphorus, Plumbum metallicum).

What is the active ingredient?

Aconitum napellus whole, Amanita muscaria fruiting body, Onion, Arnica montana whole, Arabica coffee bean, Hypericum perforatum whole, Lycopodium clavatum spore, Mercurius solubilis, Phosphorus, Lead.

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 Numbness 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.

Numbness HP NDC 44911-0625 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0625Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0625Add 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
44911-0625-1	4491106250144911062501	30 mL in 1 BOTTLE, DROPPER (44911-0625-1)Marketed from May 26, 2021

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): Numbness HP
Generic name (nonproprietary): aconitum napellus, agaricus muscarius, allium cepa, arnica montana, coffea cruda, hypericum perforatum, lycopodium clavatum, mercurius solubilis, phosphorus, plumbum metallicum
Active ingredients: Aconitum napellus whole — 30 [hp_X]/mLAmanita muscaria fruiting body — 30 [hp_X]/mLOnion — 30 [hp_X]/mLArnica montana whole — 30 [hp_X]/mLArabica coffee bean — 30 [hp_X]/mLHypericum perforatum whole — 30 [hp_X]/mLLycopodium clavatum spore — 30 [hp_X]/mLMercurius solubilis — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLLead — 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 26, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 44911-0625_9aec25cf-ef9c-417f-b225-db8a2a20306dSPL ID 9aec25cf-ef9c-417f-b225-db8a2a20306dSPL set ID 0c4ba547-b4b4-41d0-8a6b-1141ff5f9453UNII U0NQ8555JD, DIF093I037, 492225Q21H, O80TY208ZW, 3SW678MX72, XK4IUX8MNB, C88X29Y479, 324Y4038G2, 27YLU75U4W, 2P299V784PUPC 0363113700299
Pharmacologic class: Non-Standardized Food Allergenic Extract; 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

N444911062501 followed by a unit qualifier and the quantity

Package 44911-0625-01. 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 numbness, tingling, and irritation of nerves.** **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 44911-0625

What is NDC 44911-0625?: 44911-0625 is the product NDC for Numbness HP, Aconitum napellus whole 30 [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?: Numbness HP (Aconitum napellus, Agaricus muscarius, Allium cepa, Arnica montana, Coffea cruda, Hypericum perforatum, Lycopodium clavatum, Mercurius solubilis, Phosphorus, Plumbum metallicum).
What is the active ingredient?: Aconitum napellus whole, Amanita muscaria fruiting body, Onion, Arnica montana whole, Arabica coffee bean, Hypericum perforatum whole, Lycopodium clavatum spore, Mercurius solubilis, Phosphorus, Lead.
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 Numbness 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.