United States · FDA National Drug Code directory

Mytox

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
83027-0092_9b5cf627-6fce-485d-8a4c-dd1d6f32fe0f
Product NDC
83027-0092
Form
SPRAY
Composition / generic term
Borax, Colchicum Autumnale, Drosera (Rotundifolia), Arsenicum Album, Ubidecarenonum, Agaricus Muscarius, Bufo Rana
Labeler
Nutritional Specialties, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20230802
Source listing expiry
20261231

Source-listed ingredients

  • SODIUM BORATE — 4 [hp_X]/mL
  • COLCHICUM AUTUMNALE BULB — 4 [hp_X]/mL
  • DROSERA ROTUNDIFOLIA WHOLE — 6 [hp_X]/mL
  • ARSENIC TRIOXIDE — 8 [hp_X]/mL
  • UBIDECARENONE — 8 [hp_X]/mL
  • AMANITA MUSCARIA FRUITING BODY — 12 [hp_X]/mL
  • BUFO BUFO CUTANEOUS GLAND — 12 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 mL in 1 BOTTLE, SPRAY (83027-0092-1) · 83027-0092-1

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →