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D-8

Active substance: SPONGIA OFFICINALIS SKELETON, ROASTED, CAUSTICUM, LACHESIS MUTA VENOM, CALCIUM SULFIDE, THYMUS SERPYLLUM, ANTIMONY POTASSIUM TARTRATE, ACONITUM NAPELLUS, DROSERA ROTUNDIFOLIA

SOLUTION · SPONGIA OFFICINALIS SKELETON, ROASTED 4 [hp_X]/mL, CAUSTICUM 6 [hp_X]/mL, LACHESIS MUTA VENOM 8 [hp_X]/mL, CALCIUM SULFIDE 5 [hp_X]/mL, THYMUS SERPYLLUM 3 [hp_X]/mL, ANTIMONY POTASSIUM TARTRATE 6 [hp_X]/mL, ACONITUM NAPELLUS 6 [hp_X]/mL, DROSERA ROTUNDIFOLIA 4 [hp_X]/mL

United StatesActive

Marketing holder: DNA Labs, Inc.

Verified 2026-10-09 · openFDA NDC

Composition
  • SPONGIA OFFICINALIS SKELETON, ROASTED · 4 [hp_X]/mL
  • CAUSTICUM · 6 [hp_X]/mL
  • LACHESIS MUTA VENOM · 8 [hp_X]/mL
  • CALCIUM SULFIDE · 5 [hp_X]/mL
  • THYMUS SERPYLLUM · 3 [hp_X]/mL
  • ANTIMONY POTASSIUM TARTRATE · 6 [hp_X]/mL
  • ACONITUM NAPELLUS · 6 [hp_X]/mL
  • DROSERA ROTUNDIFOLIA · 4 [hp_X]/mL
Registration
Registration number
58264-0008
Registration status
Active
Dispensing
Over the counter
Route
SUBLINGUAL
Sources
  • product · openFDA NDC · 58264-0008 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 58264-0008 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 58264-0008 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 58264-0008 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 58264-0008 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 58264-0008 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 58264-0008 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 58264-0008 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 58264-0008 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 58264-0008 · Verified 2026-10-09 · open in source