Baby Nighttime Oral Pain Relief
Active substance: OYSTER SHELL CALCIUM CARBONATE, CRUDE, TRIBASIC CALCIUM PHOSPHATE, MATRICARIA CHAMOMILLA, SILICON DIOXIDE, ARNICA MONTANA, FERROSOFERRIC PHOSPHATE, ARABICA COFFEE BEAN, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
TABLET · OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/g, TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/g, MATRICARIA CHAMOMILLA 12 [hp_X]/g, SILICON DIOXIDE 12 [hp_X]/g, ARNICA MONTANA 30 [hp_X]/g, FERROSOFERRIC PHOSPHATE 12 [hp_X]/g, ARABICA COFFEE BEAN 6 [hp_X]/g, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 12 [hp_X]/g
United StatesActive
Marketing holder: Hyland' Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- OYSTER SHELL CALCIUM CARBONATE, CRUDE · 12 [hp_X]/g
- TRIBASIC CALCIUM PHOSPHATE · 12 [hp_X]/g
- MATRICARIA CHAMOMILLA · 12 [hp_X]/g
- SILICON DIOXIDE · 12 [hp_X]/g
- ARNICA MONTANA · 30 [hp_X]/g
- FERROSOFERRIC PHOSPHATE · 12 [hp_X]/g
- ARABICA COFFEE BEAN · 6 [hp_X]/g
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE · 12 [hp_X]/g
Registration
- Registration number
- 54973-3324
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 54973-3324 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 54973-3324 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 54973-3324 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 54973-3324 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 54973-3324 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 54973-3324 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 54973-3324 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 54973-3324 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 54973-3324 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 54973-3324 · Verified 2026-10-09 · open in source