NDC 43857-0523 – Androtox

Echinacea Angustifolia Whole 3 [hp_X]/mL; Centella Asiatica Whole 3 [hp_X]/mL; Saw Palmetto 3 [hp_X]/mL; Tabebuia Impetiginosa Bark 3 [hp_X]/mL; Thuja… · Liquid · Oral

Human Otc Drug

Product NDC43857-0523

Product details

Brand name
Androtox
Generic name
Echinacea (Angustifolia), Hydrocotyle Asiatica, Sabal Serrulata, Tabebuia Impetiginosa, Thuja Occidentalis, Astragalus Membranaceus, Glandula Suprarenalis Suis, Lymph Node (Suis), Zincum Gluconicum, Juniperus Virginiana, Mercurius Solubilis, Natrum Sulphuricum, Orchitinum (Suis), Prostate (Suis), Pulsatilla (Pratensis), Rhododendron Chrysanthum, Spongia Tosta, Calcarea Sulphurica, Lycopodium Clavatum, Phosphorus, Botulinum, Escherichia Coli, Proteus (Vulgaris), Pseudomonas Aeruginosa, Salmonella
Labeler
BioActive Nutritional, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
August 29, 2019
Listing expires
December 31, 2026
Pharmacologic class
Acetylcholine Release Inhibitor; Blood Coagulation Factor; Copper Absorption Inhibitor; Neuromuscular Blocker; Phosphate Binder

Active ingredients

Uses, dosage, side effects and warnings for Androtox →

Package NDC codes (1)

Package NDCDescriptionSince
43857-0523-130 mL in 1 BOTTLE, DROPPER (43857-0523-1)Aug 29, 2019