Boneforce HP
Active substance: OYSTER SHELL CALCIUM CARBONATE, CRUDE, CALCIUM FLUORIDE, TRIBASIC CALCIUM PHOSPHATE, HEKLA LAVA, HYDROFLUORIC ACID, TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, COMFREY ROOT
LIQUID · OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/mL, CALCIUM FLUORIDE 30 [hp_X]/mL, TRIBASIC CALCIUM PHOSPHATE 30 [hp_X]/mL, HEKLA LAVA 30 [hp_X]/mL, HYDROFLUORIC ACID 30 [hp_X]/mL, TOXICODENDRON PUBESCENS LEAF 30 [hp_X]/mL, SILICON DIOXIDE 30 [hp_X]/mL, COMFREY ROOT 30 [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
- OYSTER SHELL CALCIUM CARBONATE, CRUDE · 30 [hp_X]/mL
- CALCIUM FLUORIDE · 30 [hp_X]/mL
- TRIBASIC CALCIUM PHOSPHATE · 30 [hp_X]/mL
- HEKLA LAVA · 30 [hp_X]/mL
- HYDROFLUORIC ACID · 30 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF · 30 [hp_X]/mL
- SILICON DIOXIDE · 30 [hp_X]/mL
- COMFREY ROOT · 30 [hp_X]/mL
Registration
- Registration number
- 43857-0591
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 43857-0591 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 43857-0591 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 43857-0591 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 43857-0591 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 43857-0591 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 43857-0591 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 43857-0591 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 43857-0591 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 43857-0591 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 43857-0591 · Verified 2026-10-09 · open in source