United States · FDA National Drug Code directory

Menotone

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
44911-0258_1bcab3ae-97c9-492f-81f5-cdf97069980d
Product NDC
44911-0258
Form
LIQUID
Composition / generic term
Angelica Archangelica, Cimicifuga Racemosa, Belladonna, Lachesis Mutus, Pulsatilla (Pratensis), Sabina, Sanguinaria Canadensis, Sepia, Sulphur
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20150904
Source listing expiry
20261231

Source-listed ingredients

  • ANGELICA ARCHANGELICA ROOT — 3 [hp_X]/mL
  • BLACK COHOSH — 3 [hp_X]/mL
  • ATROPA BELLADONNA — 12 [hp_X]/mL
  • LACHESIS MUTA VENOM — 12 [hp_X]/mL
  • PULSATILLA PRATENSIS WHOLE — 12 [hp_X]/mL
  • JUNIPERUS SABINA LEAFY TWIG — 12 [hp_X]/mL
  • SANGUINARIA CANADENSIS ROOT — 12 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE — 12 [hp_X]/mL
  • SULFUR — 12 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 mL in 1 BOTTLE, DROPPER (44911-0258-1) · 44911-0258-1

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →