United States · FDA National Drug Code directory

SEPIA PLEX

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
62106-0117_c72dc8a8-5a42-fb8c-e053-2a95a90a9e5f
Product NDC
62106-0117
Form
LIQUID
Composition / generic term
Aconitum napellus, Cimicifuga racemosa, Lachesis mutus, Melissa officinalis, Platinum metallicum, Sanguinaria canadensis, Sepia, Sulphuricum acidum, Valeriana officinalis
Labeler
Seroyal USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20170403
Source listing expiry
20261231

Source-listed ingredients

  • BLACK COHOSH — 3 [hp_X]/30mL
  • LACHESIS MUTA VENOM — 8 [hp_X]/30mL
  • PLATINUM — 8 [hp_X]/30mL
  • SANGUINARIA CANADENSIS ROOT — 3 [hp_X]/30mL
  • SEPIA OFFICINALIS JUICE — 3 [hp_X]/30mL
  • MELISSA OFFICINALIS — 2 [hp_X]/30mL
  • SULFURIC ACID — 6 [hp_X]/30mL
  • VALERIAN — 6 [hp_X]/30mL
  • ACONITUM NAPELLUS — 6 [hp_X]/30mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, GLASS in 1 CARTON (62106-0117-0) / 30 mL in 1 BOTTLE, GLASS · 62106-0117-0

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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