D-46
Active substance: FERROSOFERRIC PHOSPHATE, LITHIUM CARBONATE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, RHODODENDRON AUREUM LEAF, FILIPENDULA ULMARIA ROOT
SOLUTION · FERROSOFERRIC PHOSPHATE 12 [hp_X]/mL, LITHIUM CARBONATE 12 [hp_X]/mL, SODIUM SULFATE 30 [hp_X]/mL, STRYCHNOS NUX-VOMICA SEED 30 [hp_X]/mL, RHODODENDRON AUREUM LEAF 6 [hp_X]/mL, FILIPENDULA ULMARIA ROOT 12 [hp_X]/mL
United StatesActive
Marketing holder: DNA Labs, Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
Composition
- FERROSOFERRIC PHOSPHATE · 12 [hp_X]/mL
- LITHIUM CARBONATE · 12 [hp_X]/mL
- SODIUM SULFATE · 30 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED · 30 [hp_X]/mL
- RHODODENDRON AUREUM LEAF · 6 [hp_X]/mL
- FILIPENDULA ULMARIA ROOT · 12 [hp_X]/mL
Registration
- Registration number
- 58264-0046
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- SUBLINGUAL
Sources
- product · openFDA NDC · 58264-0046 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 58264-0046 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 58264-0046 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 58264-0046 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 58264-0046 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 58264-0046 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 58264-0046 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 58264-0046 · Verified 2026-10-09 · open in source