Real Relief
Active substance: ARNICA MONTANA, BRYONIA ALBA ROOT, CAUSTICUM, CINCHONA OFFICINALIS BARK, SOLANUM DULCAMARA TOP, GOLDENSEAL, POTASSIUM BROMIDE, SULFUR
TABLET · ARNICA MONTANA 8 [hp_X]/1, BRYONIA ALBA ROOT 8 [hp_X]/1, CAUSTICUM 8 [hp_X]/1, CINCHONA OFFICINALIS BARK 8 [hp_X]/1, SOLANUM DULCAMARA TOP 8 [hp_X]/1, GOLDENSEAL 8 [hp_X]/1, POTASSIUM BROMIDE 8 [hp_X]/1, SULFUR 8 [hp_X]/1
United StatesActive
Marketing holder: Homeolab International (Canada) inc
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- ARNICA MONTANA · 8 [hp_X]/1
- BRYONIA ALBA ROOT · 8 [hp_X]/1
- CAUSTICUM · 8 [hp_X]/1
- CINCHONA OFFICINALIS BARK · 8 [hp_X]/1
- SOLANUM DULCAMARA TOP · 8 [hp_X]/1
- GOLDENSEAL · 8 [hp_X]/1
- POTASSIUM BROMIDE · 8 [hp_X]/1
- SULFUR · 8 [hp_X]/1
Registration
- Registration number
- 71971-6032
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 71971-6032 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 71971-6032 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 71971-6032 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 71971-6032 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 71971-6032 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 71971-6032 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 71971-6032 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 71971-6032 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 71971-6032 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 71971-6032 · Verified 2026-10-09 · open in source