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Luffa

Active substance: LUFFA ACUTANGULA FRUIT, GOLDENSEAL, MERCURIC SULFIDE, ONION, SODIUM CHLORIDE, PHOSPHORUS, EUPATORIUM PERFOLIATUM FLOWERING TOP, LOBARIA PULMONARIA

TABLET, ORALLY DISINTEGRATING · LUFFA ACUTANGULA FRUIT 6 [hp_X]/1, GOLDENSEAL 4 [hp_X]/1, MERCURIC SULFIDE 4 [hp_X]/1, ONION 6 [hp_X]/1, SODIUM CHLORIDE 6 [hp_X]/1, PHOSPHORUS 6 [hp_X]/1, EUPATORIUM PERFOLIATUM FLOWERING TOP 5 [hp_X]/1, LOBARIA PULMONARIA 2 [hp_X]/1

United StatesActive

Marketing holder: Marco Pharma International LLC.

Verified 2026-10-09 · openFDA NDC

Composition
  • LUFFA ACUTANGULA FRUIT · 6 [hp_X]/1
  • GOLDENSEAL · 4 [hp_X]/1
  • MERCURIC SULFIDE · 4 [hp_X]/1
  • ONION · 6 [hp_X]/1
  • SODIUM CHLORIDE · 6 [hp_X]/1
  • PHOSPHORUS · 6 [hp_X]/1
  • EUPATORIUM PERFOLIATUM FLOWERING TOP · 5 [hp_X]/1
  • LOBARIA PULMONARIA · 2 [hp_X]/1
Registration
Registration number
60986-2025
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 60986-2025 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 60986-2025 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 60986-2025 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 60986-2025 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 60986-2025 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 60986-2025 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 60986-2025 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 60986-2025 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 60986-2025 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 60986-2025 · Verified 2026-10-09 · open in source