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D-93

Active substance: POTASSIUM ACETATE, ANTIMONY TRISULFIDE, SAFFRON, UMBILICUS RUPESTRIS, CORALLIUM RUBRUM EXOSKELETON, BOS TAURUS PANCREAS, QUERCUS ALBA WOOD

SOLUTION · POTASSIUM ACETATE 6 [hp_X]/mL, ANTIMONY TRISULFIDE 30 [hp_X]/mL, SAFFRON 6 [hp_X]/mL, UMBILICUS RUPESTRIS 30 [hp_X]/mL, CORALLIUM RUBRUM EXOSKELETON 10 [hp_X]/mL, BOS TAURUS PANCREAS 15 [hp_X]/mL, QUERCUS ALBA WOOD 30 [hp_X]/mL

United StatesActive

Marketing holder: DNA Labs, Inc.

Verified 2026-10-09 · openFDA NDC

Composition
  • POTASSIUM ACETATE · 6 [hp_X]/mL
  • ANTIMONY TRISULFIDE · 30 [hp_X]/mL
  • SAFFRON · 6 [hp_X]/mL
  • UMBILICUS RUPESTRIS · 30 [hp_X]/mL
  • CORALLIUM RUBRUM EXOSKELETON · 10 [hp_X]/mL
  • BOS TAURUS PANCREAS · 15 [hp_X]/mL
  • QUERCUS ALBA WOOD · 30 [hp_X]/mL
Registration
Registration number
58264-0099
Registration status
Active
Dispensing
Over the counter
Route
SUBLINGUAL
Sources
  • product · openFDA NDC · 58264-0099 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 58264-0099 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 58264-0099 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 58264-0099 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 58264-0099 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 58264-0099 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 58264-0099 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 58264-0099 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 58264-0099 · Verified 2026-10-09 · open in source