Menotone NDC 44911-0258

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0258Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0258Add 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
44911-0258-1	44911025801	30 mL in 1 BOTTLE, DROPPER (44911-0258-1)Marketed from Sep 4, 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): Menotone
Generic name (nonproprietary): angelica archangelica, cimicifuga racemosa, belladonna, lachesis mutus, pulsatilla (pratensis), sabina, sanguinaria canadensis, sepia, sulphur
Active ingredients: Angelica archangelica root — 3 [hp_X]/mLBlack cohosh — 3 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLJuniperus sabina leafy twig — 12 [hp_X]/mLSanguinaria canadensis root — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLSulfur — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 4, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0258_1bcab3ae-97c9-492f-81f5-cdf97069980dSPL ID 1bcab3ae-97c9-492f-81f5-cdf97069980dSPL set ID 0921be57-44b4-4d1c-a50a-7886fc807d00UNII DTN01M69SN, K73E24S6X9, WQZ3G9PF0H, VSW71SS07I, 8E272251DI, Z5BEX9K2G1, N9288CD508, QDL83WN8C2, 70FD1KFU70

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

N444911025801 followed by a unit qualifier and the quantity

Package 44911-0258-01. 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 Jan 23, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve flushes of heat with attacks of perspiration, headaches, and moodiness with symptoms ever changing.** **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)