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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