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
- 72968-0003_f5ad27ec-888c-49f0-ac00-2a10cbf72cc3
- Product NDC
- 72968-0003
- 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)
- 20220711
- Source listing expiry
- 20271231
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
- SODIUM CHLORIDE — 30 [hp_X]/1
- SEPIA OFFICINALIS JUICE — 30 [hp_X]/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET in 1 BOTTLE, PLASTIC (72968-0003-1) · 72968-0003-1
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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