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Low Back Pain Drops 2041

Active substance: APIS MELLIFERA, BERBERIS VULGARIS ROOT BARK, BOS TAURUS HYPOTHALAMUS, POTASSIUM DICHROMATE, BOS TAURUS BONE MARROW, LYCOPODIUM CLAVATUM SPORE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, BOS TAURUS SOMATIC NERVE, SEPIA OFFICINALIS JUICE, ACONITUM NAPELLUS WHOLE, AMARYLLIS BELLADONNA WHOLE, CAUSTICUM, TOXICODENDRON PUBESCENS LEAF, ARNICA MONTANA WHOLE, ATROPINE, GRAPHITE, HYPERICUM PERFORATUM WHOLE

LIQUID · APIS MELLIFERA 6 [hp_X]/59mL, BERBERIS VULGARIS ROOT BARK 6 [hp_X]/59mL, BOS TAURUS HYPOTHALAMUS 6 [hp_X]/59mL, POTASSIUM DICHROMATE 6 [hp_X]/59mL, BOS TAURUS BONE MARROW 6 [hp_X]/59mL, LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/59mL, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 6 [hp_X]/59mL, BOS TAURUS SOMATIC NERVE 6 [hp_X]/59mL, SEPIA OFFICINALIS JUICE 6 [hp_X]/59mL, ACONITUM NAPELLUS WHOLE 6 [hp_X]/59mL, AMARYLLIS BELLADONNA WHOLE 6 [hp_X]/59mL, CAUSTICUM 6 [hp_X]/59mL, TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/59mL, ARNICA MONTANA WHOLE 6 [hp_X]/59mL, ATROPINE 12 [hp_X]/59mL, GRAPHITE 12 [hp_X]/59mL, HYPERICUM PERFORATUM WHOLE 30 [hp_X]/59mL

United StatesActive

Marketing holder: Professional Complementary Health Formulas

Verified 2026-10-09 · openFDA NDC

Composition
  • APIS MELLIFERA · 6 [hp_X]/59mL
  • BERBERIS VULGARIS ROOT BARK · 6 [hp_X]/59mL
  • BOS TAURUS HYPOTHALAMUS · 6 [hp_X]/59mL
  • POTASSIUM DICHROMATE · 6 [hp_X]/59mL
  • BOS TAURUS BONE MARROW · 6 [hp_X]/59mL
  • LYCOPODIUM CLAVATUM SPORE · 6 [hp_X]/59mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE · 6 [hp_X]/59mL
  • BOS TAURUS SOMATIC NERVE · 6 [hp_X]/59mL
  • SEPIA OFFICINALIS JUICE · 6 [hp_X]/59mL
  • ACONITUM NAPELLUS WHOLE · 6 [hp_X]/59mL
  • AMARYLLIS BELLADONNA WHOLE · 6 [hp_X]/59mL
  • CAUSTICUM · 6 [hp_X]/59mL
  • TOXICODENDRON PUBESCENS LEAF · 6 [hp_X]/59mL
  • ARNICA MONTANA WHOLE · 6 [hp_X]/59mL
  • ATROPINE · 12 [hp_X]/59mL
  • GRAPHITE · 12 [hp_X]/59mL
  • HYPERICUM PERFORATUM WHOLE · 30 [hp_X]/59mL
Registration
Registration number
63083-2041
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.9 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.10 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.11 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.12 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.13 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.14 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.15 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source
  • ingredients.16 · openFDA NDC · 63083-2041 · Verified 2026-10-09 · open in source