NDC 43857-0655 – Renotox

Triticum Aestivum Whole 1 [hp_X]/mL; Asparagus 3 [hp_X]/mL; Berberis Vulgaris Root Bark 3 [hp_X]/mL; Echinacea Angustifolia Whole 3 [hp_X]/mL; Potassium… · Liquid · Oral

Human Otc Drug

Product NDC43857-0655

Product details

Brand name
Renotox
Generic name
Triticum Aestivum, Asparagus Officinalis, Berberis Vulgaris, Echinacea (Angustifolia), Kali Muriaticum, Petroselinum Sativum, Sabal Serrulata, Solidago Virgaurea, Taraxacum Officinale, Uva-Ursi, Barosma (Betulina), Eupatorium Purpureum, Kidney (Suis), Bryonia (Alba), Mercurius Corrosivus, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicu
Labeler
BioActive Nutritional, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
March 20, 2025
Listing expires
December 31, 2026
Pharmacologic class
Acetylcholine Release Inhibitor; Copper-containing Intrauterine Device; Mood Stabilizer; Neuromuscular Blocker; Non-Standardized Food Allergenic Extract; Osmotic Laxative; Potassium Salt; Standardized Chemical Allergen; Standardized Chemical Allergen; Standardized Chemical Allergen; Standardized Chemical Allergen

Active ingredients

Uses, dosage, side effects and warnings for Renotox →

Package NDC codes (1)

Package NDCDescriptionSince
43857-0655-160 mL in 1 BOTTLE, DROPPER (43857-0655-1)Mar 20, 2025

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