Mentox HP NDC 44911-0299

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0299Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0299Add 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
44911-0299-1	44911029901	30 mL in 1 BOTTLE, DROPPER (44911-0299-1)Marketed from Nov 18, 2015

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): Mentox HPSuffix: HP
Generic name (nonproprietary): aurum metallicum, baryta carbonica, calcarea carbonica, lachesis mutus, lycopodium clavatum, natrum muriaticum, nux vomica, phosphorus
Active ingredients: Gold — 30 [hp_X]/mLBarium carbonate — 30 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLLachesis muta venom — 30 [hp_X]/mLLycopodium clavatum spore — 30 [hp_X]/mLSodium chloride — 30 [hp_X]/mLStrychnos nux-vomica seed — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 18, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 44911-0299_781fa4c6-d8d7-49c9-8e36-a5f6d8f3638cSPL ID 781fa4c6-d8d7-49c9-8e36-a5f6d8f3638cSPL set ID ebb23637-4931-4563-ab30-99bea0276580UNII 79Y1949PYO, 6P669D8HQ8, 2E32821G6I, VSW71SS07I, C88X29Y479, 451W47IQ8X, 269XH13919, 27YLU75U4W
Pharmacologic class: Non-Standardized Plant Allergenic Extract; Standardized Chemical Allergen

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

N444911029901 followed by a unit qualifier and the quantity

Package 44911-0299-01. 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 May 28, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve mental confusion, forgetfulness, and tendency toward melancholy.** **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)