NDC 43857-0632 – Neurotox

Amanita Muscaria Fruiting Body 12 [hp_X]/mL; Protortonia Cacti 12 [hp_X]/mL; Conium Maculatum Flowering Top 12 [hp_X]/mL; Lycopodium Clavatum Spore 12… · Liquid · Oral

Human Otc Drug

Product NDC43857-0632

Product details

Brand name
Neurotox
Generic name
Agaricus Muscarius, Coccus Cacti, Conium Maculatum, Lycopodium Clavatum, Phosphorus, Aluminium Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Metallicum, Ferrum Metallicum, Gadolinium Metallicum, Germanium Sesquioxide,
Labeler
BioActive Nutritional, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
August 9, 2023
Marketing end
May 25, 2028
Pharmacologic class
Acetylcholine Release Inhibitor; Copper-containing Intrauterine Device; Mood Stabilizer; Neuromuscular Blocker; Standardized Chemical Allergen; Standardized Chemical Allergen; Standardized Chemical Allergen; Standardized Chemical Allergen

Active ingredients

Uses, dosage, side effects and warnings for Neurotox →

Package NDC codes (1)

Package NDCDescriptionSince
43857-0632-160 mL in 1 BOTTLE, DROPPER (43857-0632-1)Aug 9, 2023

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