NDC 43857-0593 – Dentox

Berberis Vulgaris Root Bark 3 [hp_X]/mL; Glycyrrhiza Glabra 3 [hp_X]/mL; Arctium Lappa Root 3 [hp_X]/mL; Stillingia Sylvatica Root 3 [hp_X]/mL; Trifolium… · Liquid · Oral

Human Otc Drug

Product NDC43857-0593

Product details

Brand name
Dentox
Generic name
Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Trifolium Pratense, Phytolacca Decandra, Lymph Node(Suis), Medulla Ossis Suis, Thymus (Suis), Thyroidinum (Suis), Calcarea Fluorica, Natrum Fluoratum, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Eugenol, Formalinum, Lidocaine, Mercurius Solubilis, Molybdenum, Niccolum Metallicum, Palladium Metallicum, Stannum Metallicum, Titanium Metallicum, Zincum Metallicum
Labeler
BioActive Nutritional, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
February 14, 2023
Listing expires
December 31, 2027
Pharmacologic class
Amide Local Anesthetic; Antiarrhythmic; Copper-containing Intrauterine Device; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Standardized Chemical Allergen; Standardized Chemical Allergen; Standardized Chemical Allergen

Active ingredients

Uses, dosage, side effects and warnings for Dentox →

Package NDC codes (1)

Package NDCDescriptionSince
43857-0593-130 mL in 1 BOTTLE, DROPPER (43857-0593-1)Feb 14, 2023