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Radiation Plus

Active substance: CHONDRUS CRISPUS, FUCUS VESICULOSUS, SUS SCROFA THYROID, CADMIUM IODIDE, CADMIUM SULFIDE, IODINE, RADIUM BROMIDE, STRONTIUM CARBONATE, URANYL NITRATE HEXAHYDRATE, ALCOHOL, X-RAY EXPOSED (1000 RAD), ARNICA MONTANA

LIQUID · CHONDRUS CRISPUS 3 [hp_X]/mL, FUCUS VESICULOSUS 3 [hp_X]/mL, SUS SCROFA THYROID 8 [hp_X]/mL, CADMIUM IODIDE 12 [hp_X]/mL, CADMIUM SULFIDE 12 [hp_X]/mL, IODINE 12 [hp_X]/mL, RADIUM BROMIDE 12 [hp_X]/mL, STRONTIUM CARBONATE 12 [hp_X]/mL, URANYL NITRATE HEXAHYDRATE 12 [hp_X]/mL, ALCOHOL, X-RAY EXPOSED (1000 RAD) 30 [hp_X]/mL, ARNICA MONTANA 30 [hp_C]/mL

United StatesActive

Marketing holder: Deseret Biologicals, Inc.

Verified 2026-10-09 · openFDA NDC

Composition
Registration
Registration number
43742-0945
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 43742-0945 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 43742-0945 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 43742-0945 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 43742-0945 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 43742-0945 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 43742-0945 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 43742-0945 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 43742-0945 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 43742-0945 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 43742-0945 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 43742-0945 · Verified 2026-10-09 · open in source
  • ingredients.9 · openFDA NDC · 43742-0945 · Verified 2026-10-09 · open in source
  • ingredients.10 · openFDA NDC · 43742-0945 · Verified 2026-10-09 · open in source