Luffa is a Oral Tablet, Orally Disintegrating in the Human Otc Drug category. It is labeled and distributed by Marco Pharma International Llc.. The primary component is Luffa Acutangula Fruit; Goldenseal; Mercuric Sulfide; Onion; Sodium Chloride; Phosphorus; Eupatorium Perfoliatum Flowering Top; Lobaria Pulmonaria.
| Product ID | 60986-2025_b5ad9669-2460-6c63-e053-2995a90a1061 |
| NDC | 60986-2025 |
| Product Type | Human Otc Drug |
| Proprietary Name | Luffa |
| Generic Name | Luffa, Hydrastis Canadensis, Mercurius Sulph. Rub, Allium Cepa, Natrum Muriticum, Phosphorus, Eupatorium Perf, Sticta |
| Dosage Form | Tablet, Orally Disintegrating |
| Route of Administration | ORAL |
| Marketing Start Date | 1992-03-01 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Marco Pharma International LLC. |
| Substance Name | LUFFA ACUTANGULA FRUIT; GOLDENSEAL; MERCURIC SULFIDE; ONION; SODIUM CHLORIDE; PHOSPHORUS; EUPATORIUM PERFOLIATUM FLOWERING TOP; LOBARIA PULMONARIA |
| Active Ingredient Strength | 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 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2018-02-28 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-02-28 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| LUFFA ACUTANGULA FRUIT | 6 [hp_X]/1 |
| SPL SET ID: | 7dbb79de-c3f5-4245-884a-a6bd29bb861c |
| Manufacturer | |
| UNII |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LUFFA 78393010 not registered Dead/Abandoned |
H.H. Brown Shoe Technologies, Inc. 2004-03-30 |
![]() LUFFA 76412024 not registered Dead/Abandoned |
Edmonds, Mary Katherine 2002-05-24 |