Tri-Relief Antifungal

NDC 51393-7621 · Forces of Nature

Generic nameSODIUM CHLORIDE, SILICON DIOXIDE, and THUJA OCCIDENTALIS LEAFY TWIG

Dosage formSOLUTION/ DROPS

RouteTOPICAL

Active ingredient(s)SODIUM CHLORIDE, SILICON DIOXIDE, THUJA OCCIDENTALIS LEAFY TWIG

Strength10; 10; 10 [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL

Pharmacologic classIncreased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]

Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

51393-7621-4 — 1 BOTTLE, DISPENSING in 1 CARTON (51393-7621-4) / 4 mL in 1 BOTTLE, DISPENSING

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51393-5008 — Urtica Dioica Leaf, Inula Helenium Root, Angelica Archangelica Root, Pine Needle Oil (Pinus Sylvestris), Sodium Chloride, and Althaea…, 51393-5013 — echinacea angustifolia whole, sodium chloride, thuja occidentalis leafy twig, and calendula officinalis flowering top, 51393-5622 — Centella Asiatica, Iris Versicolor Root, Arctium Lappa Root, Sodium Chloride, Ruta Graveolens Flowering Top, Silicon Dioxide, Taraxacum…, 51393-6112 — Calendula Officinalis Flowering Top and Silicon Dioxide, 51393-6988 — Calendula Officinalis Flowering Top and Silicon Dioxide, 51393-6989 — Calendula Officinalis Flowering Top, Silicon Dioxide, and Hypericum Perforatum, 51393-7112 — Calendula Officinalis Flowering Top, Allylthiourea, and Silicon Dioxide, 51393-7434 — Calendula Officinalis Flowering Top, Phytolacca Americana Root, And Thuja Occidentalis Leafy Twig, 51393-7566 — Arabica Coffee Bean, Silicon Dioxide, and Hypericum Perforatum, 51393-7589 — iris versicolor root and sodium chloride, 51393-7656 — Arnica Montana, Urtica Urens, Silicon Dioxide, and Thuja Occidentalis Leaf, 51393-8200 — Arnica Montana Whole, Horse Chestnut, Hypericum Perforatum whole, Ruta Graveolens Flowering Top, and Thuja Occidentalis Leafy Twig, 51662-1257 — BACTERIOSTATIC SODIUM CHLORIDE, 51662-1259 — BACTERIOSTATIC SODIUM CHLORIDE, 51662-1342 — SODIUM CHLORIDE, 51662-1359 — 0.9% SODIUM CHLORIDE, 51662-1464 — SODIUM CHLORIDE, 51662-1516 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, 51662-1517 — 0.9% SODIUM CHLORIDE, 51662-1518 — 0.9% SODIUM CHLORIDE, +1039 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels