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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