United States · FDA National Drug Code directory

Herplex

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
72968-0004_1d44a27d-7870-4a51-88ec-195c547bbad0
Product NDC
72968-0004
Form
TABLET
Composition / generic term
Anatherum Muricatum, Clematis Erecta, Mezereum, Phytolacca Decandra, Ranunculus Bulbosus, Rhus Tox, Thuja Occidentalis, Natrum Muriaticum, Sepia
Labeler
Nashco Products LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20220830
Source listing expiry
20261231

Source-listed ingredients

  • CHRYSOPOGON ZIZANIOIDES ROOT — 12 [hp_X]/1
  • CLEMATIS RECTA FLOWERING TOP — 12 [hp_X]/1
  • DAPHNE MEZEREUM BARK — 12 [hp_X]/1
  • PHYTOLACCA AMERICANA ROOT — 12 [hp_X]/1
  • RANUNCULUS BULBOSUS WHOLE — 12 [hp_X]/1
  • TOXICODENDRON PUBESCENS LEAF — 12 [hp_X]/1
  • THUJA OCCIDENTALIS LEAFY TWIG — 12 [hp_X]/1
  • SEPIA OFFICINALIS JUICE — 30 [hp_X]/1
  • SODIUM CHLORIDE — 30 [hp_X]/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 120 TABLET in 1 BOTTLE, PLASTIC (72968-0004-1) · 72968-0004-1

Source and coverage

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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.

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