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Control

Active substance: SEMECARPUS ANACARDIUM JUICE, SODIUM CHLORIDE, SILVER NITRATE, ASARUM CANADENSE ROOT, BLATTA ORIENTALIS, BUFO BUFO CUTANEOUS GLAND, SUS SCROFA CEREBRUM, CLEMATIS RECTA FLOWERING TOP, CUPRIC ACETATE, SUS SCROFA HYPOTHALAMUS, STRYCHNOS IGNATII SEED, DIBASIC POTASSIUM PHOSPHATE, LACHESIS MUTA VENOM, MERCURIUS SOLUBILIS, SODIUM SULFATE, SUS SCROFA PLACENTA, TOXICODENDRON PUBESCENS LEAF, THUJA OCCIDENTALIS LEAFY TWIG, THYMOL, VALERIAN

LIQUID · SEMECARPUS ANACARDIUM JUICE 12 [hp_X]/mL, SODIUM CHLORIDE 6 [hp_X]/mL, SILVER NITRATE 6 [hp_X]/mL, ASARUM CANADENSE ROOT 12 [hp_X]/mL, BLATTA ORIENTALIS 12 [hp_X]/mL, BUFO BUFO CUTANEOUS GLAND 12 [hp_X]/mL, SUS SCROFA CEREBRUM 6 [hp_X]/mL, CLEMATIS RECTA FLOWERING TOP 6 [hp_X]/mL, CUPRIC ACETATE 6 [hp_X]/mL, SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL, STRYCHNOS IGNATII SEED 12 [hp_X]/mL, DIBASIC POTASSIUM PHOSPHATE 6 [hp_X]/mL, LACHESIS MUTA VENOM 12 [hp_X]/mL, MERCURIUS SOLUBILIS 12 [hp_X]/mL, SODIUM SULFATE 6 [hp_X]/mL, SUS SCROFA PLACENTA 8 [hp_X]/mL, TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL, THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL, THYMOL 12 [hp_X]/mL, VALERIAN 6 [hp_X]/mL

United StatesActive

Marketing holder: Deseret Biologicals, Inc.

Verified 2026-10-09 · openFDA NDC

Composition
  • SEMECARPUS ANACARDIUM JUICE · 12 [hp_X]/mL
  • SODIUM CHLORIDE · 6 [hp_X]/mL
  • SILVER NITRATE · 6 [hp_X]/mL
  • ASARUM CANADENSE ROOT · 12 [hp_X]/mL
  • BLATTA ORIENTALIS · 12 [hp_X]/mL
  • BUFO BUFO CUTANEOUS GLAND · 12 [hp_X]/mL
  • SUS SCROFA CEREBRUM · 6 [hp_X]/mL
  • CLEMATIS RECTA FLOWERING TOP · 6 [hp_X]/mL
  • CUPRIC ACETATE · 6 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS · 8 [hp_X]/mL
  • STRYCHNOS IGNATII SEED · 12 [hp_X]/mL
  • DIBASIC POTASSIUM PHOSPHATE · 6 [hp_X]/mL
  • LACHESIS MUTA VENOM · 12 [hp_X]/mL
  • MERCURIUS SOLUBILIS · 12 [hp_X]/mL
  • SODIUM SULFATE · 6 [hp_X]/mL
  • SUS SCROFA PLACENTA · 8 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF · 12 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG · 12 [hp_X]/mL
  • THYMOL · 12 [hp_X]/mL
  • VALERIAN · 6 [hp_X]/mL
Registration
Registration number
43742-2089
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.9 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.10 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.11 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.12 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.13 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.14 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.15 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.16 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.17 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.18 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source
  • ingredients.19 · openFDA NDC · 43742-2089 · Verified 2026-10-09 · open in source