RENAFORCE
Active substance: BERBERIS VULGARIS ROOT BARK, ECHINACEA ANGUSTIFOLIA WHOLE, PROTORTONIA CACTI, POTASSIUM CHLORIDE, LYCOPODIUM CLAVATUM SPORE, NITRIC ACID
LIQUID · BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL, ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL, PROTORTONIA CACTI 12 [hp_X]/mL, POTASSIUM CHLORIDE 12 [hp_X]/mL, LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL, NITRIC ACID 12 [hp_X]/mL
United StatesActive
Marketing holder: BioActive Nutritional, Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- BERBERIS VULGARIS ROOT BARK · 3 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE · 3 [hp_X]/mL
- PROTORTONIA CACTI · 12 [hp_X]/mL
- POTASSIUM CHLORIDE · 12 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE · 12 [hp_X]/mL
- NITRIC ACID · 12 [hp_X]/mL
Registration
- Registration number
- 43857-0340
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 43857-0340 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 43857-0340 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 43857-0340 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 43857-0340 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 43857-0340 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 43857-0340 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 43857-0340 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 43857-0340 · Verified 2026-10-09 · open in source