Ring Relief
Active substance: ARNICA MONTANA, CALCIUM SULFIDE, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLUBILIS, SALICYLIC ACID, SILICON DIOXIDE, ALLYLTHIOUREA
LIQUID · ARNICA MONTANA 6 [hp_X]/mL, CALCIUM SULFIDE 13 [hp_X]/mL, HYPERICUM PERFORATUM 6 [hp_X]/mL, LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL, MERCURIUS SOLUBILIS 13 [hp_X]/mL, SALICYLIC ACID 6 [hp_X]/mL, SILICON DIOXIDE 13 [hp_X]/mL, ALLYLTHIOUREA 6 [hp_X]/mL
United StatesActive
Marketing holder: TRP Company
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- ARNICA MONTANA · 6 [hp_X]/mL
- CALCIUM SULFIDE · 13 [hp_X]/mL
- HYPERICUM PERFORATUM · 6 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE · 12 [hp_X]/mL
- MERCURIUS SOLUBILIS · 13 [hp_X]/mL
- SALICYLIC ACID · 6 [hp_X]/mL
- SILICON DIOXIDE · 13 [hp_X]/mL
- ALLYLTHIOUREA · 6 [hp_X]/mL
Registration
- Registration number
- 17312-001
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- AURICULAR (OTIC)
Sources
- product · openFDA NDC · 17312-001 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 17312-001 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 17312-001 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 17312-001 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 17312-001 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 17312-001 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 17312-001 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 17312-001 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 17312-001 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 17312-001 · Verified 2026-10-09 · open in source