Difficulty Breathing Drops 2171
Active substance: BEEF LUNG, PLANTAGO MAJOR WHOLE, BOS TAURUS INTERVERTEBRAL DISC, SILICON DIOXIDE, CONIUM MACULATUM FLOWERING TOP, ANTIMONY POTASSIUM TARTRATE, SILVER NITRATE, SELENICEREUS GRANDIFLORUS STEM, BLACK COHOSH, BEEF SHORT PLATE, MOSCHUS MOSCHIFERUS MUSK SAC RESIN, AMARYLLIS BELLADONNA WHOLE, COPPER, DAPHNE MEZEREUM BARK, TOXICODENDRON PUBESCENS LEAF, HYOSCYAMUS NIGER, DATURA STRAMONIUM
LIQUID · BEEF LUNG 6 [hp_X]/59mL, PLANTAGO MAJOR WHOLE 6 [hp_X]/59mL, BOS TAURUS INTERVERTEBRAL DISC 6 [hp_X]/59mL, SILICON DIOXIDE 8 [hp_X]/59mL, CONIUM MACULATUM FLOWERING TOP 9 [hp_X]/59mL, ANTIMONY POTASSIUM TARTRATE 12 [hp_X]/59mL, SILVER NITRATE 12 [hp_X]/59mL, SELENICEREUS GRANDIFLORUS STEM 12 [hp_X]/59mL, BLACK COHOSH 12 [hp_X]/59mL, BEEF SHORT PLATE 12 [hp_X]/59mL, MOSCHUS MOSCHIFERUS MUSK SAC RESIN 12 [hp_X]/59mL, AMARYLLIS BELLADONNA WHOLE 30 [hp_X]/59mL, COPPER 30 [hp_X]/59mL, DAPHNE MEZEREUM BARK 30 [hp_X]/59mL, TOXICODENDRON PUBESCENS LEAF 30 [hp_X]/59mL, HYOSCYAMUS NIGER 200 [hp_X]/59mL, DATURA STRAMONIUM 200 [hp_X]/59mL
United StatesActive
Marketing holder: Professional Complementary Health Formulas
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
- BEEF LUNG · 6 [hp_X]/59mL
- PLANTAGO MAJOR WHOLE · 6 [hp_X]/59mL
- BOS TAURUS INTERVERTEBRAL DISC · 6 [hp_X]/59mL
- SILICON DIOXIDE · 8 [hp_X]/59mL
- CONIUM MACULATUM FLOWERING TOP · 9 [hp_X]/59mL
- ANTIMONY POTASSIUM TARTRATE · 12 [hp_X]/59mL
- SILVER NITRATE · 12 [hp_X]/59mL
- SELENICEREUS GRANDIFLORUS STEM · 12 [hp_X]/59mL
- BLACK COHOSH · 12 [hp_X]/59mL
- BEEF SHORT PLATE · 12 [hp_X]/59mL
- MOSCHUS MOSCHIFERUS MUSK SAC RESIN · 12 [hp_X]/59mL
- AMARYLLIS BELLADONNA WHOLE · 30 [hp_X]/59mL
- COPPER · 30 [hp_X]/59mL
- DAPHNE MEZEREUM BARK · 30 [hp_X]/59mL
- TOXICODENDRON PUBESCENS LEAF · 30 [hp_X]/59mL
- HYOSCYAMUS NIGER · 200 [hp_X]/59mL
- DATURA STRAMONIUM · 200 [hp_X]/59mL
- Registration number
- 63083-2171
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
- product · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.8 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.9 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.10 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.11 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.12 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.13 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.14 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.15 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source
- ingredients.16 · openFDA NDC · 63083-2171 · Verified 2026-10-09 · open in source