United States · FDA National Drug Code directory

Luffa

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
60986-2025_483bedff-d761-3c5b-e063-6394a90a8eeb
Product NDC
60986-2025
Form
TABLET, ORALLY DISINTEGRATING
Composition / generic term
Luffa, Hydrastis Canadensis, Mercurius Sulph. Rub, Allium Cepa, Natrum Muriticum, Phosphorus, Eupatorium Perf, Sticta
Labeler
Marco Pharma International LLC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
19920301
Source listing expiry
20271231

Source-listed ingredients

  • 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

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (60986-2025-2) · 60986-2025-2

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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