NDC 60986-2025 – Luffa

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;… · Tablet, Orally Disintegrating · Oral

Human Otc Drug

Product NDC60986-2025

Product details

Brand name
Luffa
Generic name
Luffa, Hydrastis Canadensis, Mercurius Sulph. Rub, Allium Cepa, Natrum Muriticum, Phosphorus, Eupatorium Perf, Sticta
Labeler
Marco Pharma International LLC.
Dosage form
Tablet, Orally Disintegrating
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
March 1, 1992
Listing expires
December 31, 2027
Pharmacologic class
Non-Standardized Food Allergenic Extract; Osmotic Laxative

Active ingredients

Uses, dosage, side effects and warnings for Luffa →

Package NDC codes (1)

Package NDCDescriptionSince
60986-2025-260 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (60986-2025-2)Feb 28, 2018