United States · FDA National Drug Code directory
Vertitone
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
- 44911-0181_2f9df577-5024-4911-9ab7-ad3387dff794
- Product NDC
- 44911-0181
- Form
- LIQUID
- Composition / generic term
- Baptisia Tinctoria, Agaricus Muscarius, Arsenicum Album, Belladonna, Calcarea Carbonica, Cocculus Indicus, Conium Maculatum, Phosphorus, Pulsatilla (Pratensis)
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20150708
- Source listing expiry
- 20261231
Source-listed ingredients
- BAPTISIA TINCTORIA ROOT — 3 [hp_X]/mL
- AMANITA MUSCARIA FRUITING BODY — 12 [hp_X]/mL
- ARSENIC TRIOXIDE — 12 [hp_X]/mL
- ATROPA BELLADONNA — 12 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE — 12 [hp_X]/mL
- ANAMIRTA COCCULUS SEED — 12 [hp_X]/mL
- CONIUM MACULATUM FLOWERING TOP — 12 [hp_X]/mL
- PHOSPHORUS — 12 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE — 12 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 mL in 1 BOTTLE, DROPPER (44911-0181-1) · 44911-0181-1
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 →