Rhus Aconitum
Active substance: GELSEMIUM SEMPERVIRENS ROOT, ACONITUM NAPELLUS, PSEUDOGNAPHALIUM LUTEOALBUM LEAF, MANDRAGORA OFFICINARUM ROOT, TOXICODENDRON PUBESCENS LEAF, ATROPA BELLADONNA, PENOXSULAM
PELLET · GELSEMIUM SEMPERVIRENS ROOT 3 [hp_X]/1, ACONITUM NAPELLUS 4 [hp_X]/1, PSEUDOGNAPHALIUM LUTEOALBUM LEAF 4 [hp_X]/1, MANDRAGORA OFFICINARUM ROOT 4 [hp_X]/1, TOXICODENDRON PUBESCENS LEAF 4 [hp_X]/1, ATROPA BELLADONNA 6 [hp_X]/1, PENOXSULAM 10 [hp_X]/1
United StatesActive
Marketing holder: Uriel Pharmacy Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- GELSEMIUM SEMPERVIRENS ROOT · 3 [hp_X]/1
- ACONITUM NAPELLUS · 4 [hp_X]/1
- PSEUDOGNAPHALIUM LUTEOALBUM LEAF · 4 [hp_X]/1
- MANDRAGORA OFFICINARUM ROOT · 4 [hp_X]/1
- TOXICODENDRON PUBESCENS LEAF · 4 [hp_X]/1
- ATROPA BELLADONNA · 6 [hp_X]/1
- PENOXSULAM · 10 [hp_X]/1
Registration
- Registration number
- 48951-8142
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 48951-8142 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 48951-8142 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 48951-8142 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 48951-8142 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 48951-8142 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 48951-8142 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 48951-8142 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 48951-8142 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 48951-8142 · Verified 2026-10-09 · open in source