NDC 43857-0039

Dentox

Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Phytolacca Decandra, Stillingia Sylvatica, Trifolium Pratense, Lymph Node(suis), Medulla Ossis Suis, Thymus (suis), Thyroidinum (suis),

Dentox is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Bioactive Nutritional, Inc.. The primary component is Berberis Vulgaris Root Bark; Glycyrrhiza Glabra; Arctium Lappa Root; Phytolacca Americana Root; Stillingia Sylvatica Root; Trifolium Pratense Flower; Sus Scrofa Lymph; Sus Scrofa Bone Marrow; Sus Scrofa Thymus; Thyroid, Porcine; Calcium Fluoride; Sodium Fluoride; Silver; Gold; Copper; Eugenol; Formaldehyde; Lidocaine; Mercurius Solubilis; Molybdenum; Nickel; Palladium; Tin; Titanium; Zinc.

• Product ID: 43857-0039_e4462f59-9ba5-43a9-9b2b-3e5a807545dd
• NDC: 43857-0039
• Product Type: Human Otc Drug
• Proprietary Name: Dentox
• Generic Name: Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Phytolacca Decandra, Stillingia Sylvatica, Trifolium Pratense, Lymph Node(suis), Medulla Ossis Suis, Thymus (suis), Thyroidinum (suis),
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2012-06-05
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: BioActive Nutritional, Inc.
• Substance Name: BERBERIS VULGARIS ROOT BARK; GLYCYRRHIZA GLABRA; ARCTIUM LAPPA ROOT; PHYTOLACCA AMERICANA ROOT; STILLINGIA SYLVATICA ROOT; TRIFOLIUM PRATENSE FLOWER; SUS SCROFA LYMPH; SUS SCROFA BONE MARROW; SUS SCROFA THYMUS; THYROID, PORCINE; CALCIUM FLUORIDE; SODIUM FLUORIDE; SILVER; GOLD; COPPER; EUGENOL; FORMALDEHYDE; LIDOCAINE; MERCURIUS SOLUBILIS; MOLYBDENUM; NICKEL; PALLADIUM; TIN; TITANIUM; ZINC
• Active Ingredient Strength: 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 43857-0039-1

30 mL in 1 BOTTLE, DROPPER (43857-0039-1)

• Marketing Start Date: 2016-09-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43857-0039-1 [43857003901]

Dentox LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-09-27

Drug Details

Active Ingredients

Ingredient	Strength
BERBERIS VULGARIS ROOT BARK	3 [hp_X]/mL

OpenFDA Data

• SPL SET ID: ae51c063-63b4-45cc-b8d0-e98584b65a66
• Manufacturer:
  • BioActive Nutritional, Inc.
• UNII:
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