N-13
Active substance: CEANOTHUS AMERICANUS LEAF, URTICA URENS, SODIUM CHLORIDE, LACHESIS MUTA WHOLE, CINCHONA OFFICINALIS BARK, LYCOPODIUM CLAVATUM WHOLE, FERRIC CHLORIDE HEXAHYDRATE, SUS SCROFA SPLEEN
SOLUTION · CEANOTHUS AMERICANUS LEAF 4 [hp_X]/mL, URTICA URENS 4 [hp_X]/mL, SODIUM CHLORIDE 6 [hp_X]/mL, LACHESIS MUTA WHOLE 12 [hp_X]/mL, CINCHONA OFFICINALIS BARK 8 [hp_X]/mL, LYCOPODIUM CLAVATUM WHOLE 6 [hp_X]/mL, FERRIC CHLORIDE HEXAHYDRATE 6 [hp_X]/mL, SUS SCROFA SPLEEN 200 [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
- CEANOTHUS AMERICANUS LEAF · 4 [hp_X]/mL
- URTICA URENS · 4 [hp_X]/mL
- SODIUM CHLORIDE · 6 [hp_X]/mL
- LACHESIS MUTA WHOLE · 12 [hp_X]/mL
- CINCHONA OFFICINALIS BARK · 8 [hp_X]/mL
- LYCOPODIUM CLAVATUM WHOLE · 6 [hp_X]/mL
- FERRIC CHLORIDE HEXAHYDRATE · 6 [hp_X]/mL
- SUS SCROFA SPLEEN · 200 [hp_X]/mL
Registration
- Registration number
- 58264-0211
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- SUBLINGUAL
Sources
- product · openFDA NDC · 58264-0211 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 58264-0211 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 58264-0211 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 58264-0211 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 58264-0211 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 58264-0211 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 58264-0211 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 58264-0211 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 58264-0211 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 58264-0211 · Verified 2026-10-09 · open in source