United States · FDA National Drug Code directory

Femstat C

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
44911-0607_b82b0bcb-2279-4e39-ab1b-2316f7d7ca7d
Product NDC
44911-0607
Form
LIQUID
Composition / generic term
Echinacea (Angustifolia), Fucus Vesiculosus, Hydrastis Canadensis, Phytolacca Decandra, Kreosotum, Natrum Muriaticum, Candida Albicans, Lycopodium Clavatum, Pulsatilla (Pratensis), Sepia
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20210526
Source listing expiry
20261231

Source-listed ingredients

  • ECHINACEA ANGUSTIFOLIA WHOLE — 3 [hp_X]/mL
  • FUCUS VESICULOSUS — 3 [hp_X]/mL
  • GOLDENSEAL — 6 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT — 6 [hp_X]/mL
  • WOOD CREOSOTE — 12 [hp_X]/mL
  • SODIUM CHLORIDE — 12 [hp_X]/mL
  • CANDIDA ALBICANS — 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE — 30 [hp_X]/mL
  • PULSATILLA PRATENSIS WHOLE — 30 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE — 30 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 mL in 1 BOTTLE, DROPPER (44911-0607-1) · 44911-0607-1

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 →