United States · FDA National Drug Code directory
Tri-Relief Antifungal
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
- 51393-7621_bbd2afbf-5951-471d-b3fd-923ea13bae8d
- Product NDC
- 51393-7621
- Form
- SOLUTION/ DROPS
- Composition / generic term
- SODIUM CHLORIDE, SILICON DIOXIDE, and THUJA OCCIDENTALIS LEAFY TWIG
- Labeler
- Forces of Nature
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20251101
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM CHLORIDE — 10 [hp_X]/100mL
- SILICON DIOXIDE — 10 [hp_X]/100mL
- THUJA OCCIDENTALIS LEAFY TWIG — 10 [hp_X]/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, DISPENSING in 1 CARTON (51393-7621-4) / 4 mL in 1 BOTTLE, DISPENSING · 51393-7621-4
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 →