NDC 63083-6021

Mytox 6021

Mytox

Mytox 6021 is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Professional Complementary Health Formulas. The primary component is Amanita Muscaria Fruiting Body; Arsenic Trioxide; Bufo Bufo Cutaneous Gland; Colchicum Autumnale Bulb; Drosera Rotundifolia Whole; Sodium Borate; Ubidecarenone.

• Product ID: 63083-6021_cd2ce96f-3f81-4d3a-a815-1ac05ecdb4f3
• NDC: 63083-6021
• Product Type: Human Otc Drug
• Proprietary Name: Mytox 6021
• Generic Name: Mytox
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 1984-08-15
• Marketing Category: UNAPPROVED HOMEOPATHIC /
• Labeler Name: Professional Complementary Health Formulas
• Substance Name: AMANITA MUSCARIA FRUITING BODY; ARSENIC TRIOXIDE; BUFO BUFO CUTANEOUS GLAND; COLCHICUM AUTUMNALE BULB; DROSERA ROTUNDIFOLIA WHOLE; SODIUM BORATE; UBIDECARENONE
• Active Ingredient Strength: 6 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 63083-6021-2

59 mL in 1 BOTTLE, DROPPER (63083-6021-2)

• Marketing Start Date: 1985-08-15
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details