NDC 43857-0534 – Universaltox

Alfalfa 3 [hp_X]/mL; Avena Sativa Flowering Top 3 [hp_X]/mL; Fucus Vesiculosus 4 [hp_X]/mL; Hordeum Vulgare Top 4 [hp_X]/mL; Nasturtium Officinale 4 [hp_X]/mL;… · Liquid · Oral

Human Otc Drug

Product NDC43857-0534

Product details

Brand name
Universaltox
Generic name
Alfalfa, Avena Sativa, Fucus Vesiculosus, Hordeum Vulgare, Nasturtium Aquaticum, Raphanus Sativus, Triticum Aestivum, Iodium, Ubidecarenonum, Glandula Suprarenalis Suis, Hepar Suis, Manganese Gluconate, Oryza Sativa, Thyroidinum (Suis), Calcarea Carbonica, Natrum Muriaticum, Pulsatilla (Pratensis), Rhus Tox, Cortisone Aceticum
Labeler
BioActive Nutritional, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
October 3, 2019
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid; Non-Standardized Food Allergenic Extract; Paramagnetic Contrast Agent

Active ingredients

Uses, dosage, side effects and warnings for Universaltox →

Package NDC codes (1)

Package NDCDescriptionSince
43857-0534-130 mL in 1 BOTTLE, DROPPER (43857-0534-1)Oct 3, 2019