D-59
Active substance: FUCUS VESICULOSUS, SPONGIA OFFICINALIS SKELETON, ROASTED, GRAPHITE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, SODIUM SULFATE, CROTON OIL
SOLUTION · FUCUS VESICULOSUS 3 [hp_X]/mL, SPONGIA OFFICINALIS SKELETON, ROASTED 3 [hp_X]/mL, GRAPHITE 12 [hp_X]/mL, OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL, SODIUM SULFATE 2 [hp_X]/mL, CROTON OIL 4 [hp_X]/mL
United StatesActive
Marketing holder: DNA Labs, Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- FUCUS VESICULOSUS · 3 [hp_X]/mL
- SPONGIA OFFICINALIS SKELETON, ROASTED · 3 [hp_X]/mL
- GRAPHITE · 12 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE · 12 [hp_X]/mL
- SODIUM SULFATE · 2 [hp_X]/mL
- CROTON OIL · 4 [hp_X]/mL
Registration
- Registration number
- 58264-0059
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- SUBLINGUAL
Sources
- product · openFDA NDC · 58264-0059 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 58264-0059 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 58264-0059 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 58264-0059 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 58264-0059 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 58264-0059 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 58264-0059 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 58264-0059 · Verified 2026-10-09 · open in source