United States · FDA National Drug Code directory
TOXO HOMO
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
- 43742-2002_639b723a-bdad-4e0e-9c2e-f1182f4e927c
- Product NDC
- 43742-2002
- Form
- LIQUID
- Composition / generic term
- TOXOPLASMA GONDII DNA
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20201221
- Source listing expiry
- 20261231
Source-listed ingredients
- TOXOPLASMA GONDII DNA — 15 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 mL in 1 BOTTLE, PLASTIC (43742-2002-1) · 43742-2002-1
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 →