Product NDC: | 60986-2025 |
Proprietary Name: | Luffa |
Non Proprietary Name: | Luffa, Hydrastis Canadensis, Mercurius Sulph. Rub, Allium Cepa, Natrum Muriticum, Phosphorus, Eupatorium Perf, Sticta |
Active Ingredient(s): | 5; 4; 2; 6; 4; 6; 6; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; Luffa, Hydrastis Canadensis, Mercurius Sulph. Rub, Allium Cepa, Natrum Muriticum, Phosphorus, Eupatorium Perf, Sticta |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60986-2025 |
Labeler Name: | Marco Pharma International LLC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19920301 |
Package NDC: | 60986-2025-2 |
Package Description: | 60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (60986-2025-2) |
NDC Code | 60986-2025-2 |
Proprietary Name | Luffa |
Package Description | 60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (60986-2025-2) |
Product NDC | 60986-2025 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Luffa, Hydrastis Canadensis, Mercurius Sulph. Rub, Allium Cepa, Natrum Muriticum, Phosphorus, Eupatorium Perf, Sticta |
Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
Route Name | ORAL |
Start Marketing Date | 19920301 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Marco Pharma International LLC. |
Substance Name | EUPATORIUM PERFOLIATUM FLOWERING TOP; GOLDENSEAL; LOBARIA PULMONARIA; LUFFA ACUTANGULA FRUIT; MERCURIC SULFIDE; ONION; PHOSPHORUS; SODIUM CHLORIDE |
Strength Number | 5; 4; 2; 6; 4; 6; 6; 6 |
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 |
Pharmaceutical Classes |