| NDC Code | 60986-2025-2 |
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| Package Description | 60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (60986-2025-2) |
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| Product NDC | 60986-2025 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Luffa |
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| Non-Proprietary Name | Luffa, Hydrastis Canadensis, Mercurius Sulph. Rub, Allium Cepa, Natrum Muriticum, Phosphorus, Eupatorium Perf, Sticta |
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| Dosage Form | TABLET, ORALLY DISINTEGRATING |
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| Usage | ORAL |
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| Start Marketing Date | 19920301 |
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| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
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| Manufacturer | Marco Pharma International LLC. |
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| Substance Name | EUPATORIUM PERFOLIATUM FLOWERING TOP; GOLDENSEAL; LOBARIA PULMONARIA; LUFFA ACUTANGULA FRUIT; MERCURIC SULFIDE; ONION; PHOSPHORUS; SODIUM CHLORIDE |
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| Strength | 5; 4; 2; 6; 4; 6; 6; 6 |
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| Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
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| Pharmacy Classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Non-Standardized Food Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Vegetable Proteins [CS] |
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