HPNP
Active substance: SODIUM SULFATE, ORYCTOLAGUS CUNICULUS KIDNEY, PHOSPHORIC ACID, BERBERIS VULGARIS ROOT BARK, CHELIDONIUM MAJUS ROOT, WOOD CREOSOTE, ORYCTOLAGUS CUNICULUS PANCREATIN, SYZYGIUM CUMINI FRUIT, BILBERRY
LIQUID · SODIUM SULFATE 6 [hp_X]/30mL, ORYCTOLAGUS CUNICULUS KIDNEY 10 [hp_X]/30mL, PHOSPHORIC ACID 4 [hp_X]/30mL, BERBERIS VULGARIS ROOT BARK 2 [hp_X]/30mL, CHELIDONIUM MAJUS ROOT 4 [hp_X]/30mL, WOOD CREOSOTE 6 [hp_X]/30mL, ORYCTOLAGUS CUNICULUS PANCREATIN 10 [hp_X]/30mL, SYZYGIUM CUMINI FRUIT 10 [hp_X]/30mL, BILBERRY 2 [hp_X]/30mL
United StatesActive
Marketing holder: Seroyal USA
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- SODIUM SULFATE · 6 [hp_X]/30mL
- ORYCTOLAGUS CUNICULUS KIDNEY · 10 [hp_X]/30mL
- PHOSPHORIC ACID · 4 [hp_X]/30mL
- BERBERIS VULGARIS ROOT BARK · 2 [hp_X]/30mL
- CHELIDONIUM MAJUS ROOT · 4 [hp_X]/30mL
- WOOD CREOSOTE · 6 [hp_X]/30mL
- ORYCTOLAGUS CUNICULUS PANCREATIN · 10 [hp_X]/30mL
- SYZYGIUM CUMINI FRUIT · 10 [hp_X]/30mL
- BILBERRY · 2 [hp_X]/30mL
Registration
- Registration number
- 62106-0629
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 62106-0629 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 62106-0629 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 62106-0629 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 62106-0629 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 62106-0629 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 62106-0629 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 62106-0629 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 62106-0629 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 62106-0629 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 62106-0629 · Verified 2026-10-09 · open in source
- ingredients.8 · openFDA NDC · 62106-0629 · Verified 2026-10-09 · open in source