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Mytox

Active substance: SODIUM BORATE, COLCHICUM AUTUMNALE BULB, DROSERA ROTUNDIFOLIA WHOLE, ARSENIC TRIOXIDE, UBIDECARENONE, AMANITA MUSCARIA FRUITING BODY, BUFO BUFO CUTANEOUS GLAND

SPRAY · SODIUM BORATE 4 [hp_X]/mL, COLCHICUM AUTUMNALE BULB 4 [hp_X]/mL, DROSERA ROTUNDIFOLIA WHOLE 6 [hp_X]/mL, ARSENIC TRIOXIDE 8 [hp_X]/mL, UBIDECARENONE 8 [hp_X]/mL, AMANITA MUSCARIA FRUITING BODY 12 [hp_X]/mL, BUFO BUFO CUTANEOUS GLAND 12 [hp_X]/mL

United StatesActive

Marketing holder: Nutritional Specialties, Inc.

Verified 2026-10-09 · openFDA NDC

Composition
  • SODIUM BORATE · 4 [hp_X]/mL
  • COLCHICUM AUTUMNALE BULB · 4 [hp_X]/mL
  • DROSERA ROTUNDIFOLIA WHOLE · 6 [hp_X]/mL
  • ARSENIC TRIOXIDE · 8 [hp_X]/mL
  • UBIDECARENONE · 8 [hp_X]/mL
  • AMANITA MUSCARIA FRUITING BODY · 12 [hp_X]/mL
  • BUFO BUFO CUTANEOUS GLAND · 12 [hp_X]/mL
Registration
Registration number
83027-0092
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 83027-0092 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 83027-0092 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 83027-0092 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 83027-0092 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 83027-0092 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 83027-0092 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 83027-0092 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 83027-0092 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 83027-0092 · Verified 2026-10-09 · open in source