Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Tri-Relief Antifungal NDC 51393-7621
sodium chloride, silicon dioxide, and thuja occidentalis leafy twig · Sodium chloride 10 [hp_X]/100mL + 2 more ingredients · Solution/ drops · Topical · Forces of Nature
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 51393-7621-4 | 51393762104 | 1 BOTTLE, DISPENSING in 1 CARTON (51393-7621-4) / 4 mL in 1 BOTTLE, DISPENSINGMarketed from Nov 1, 2025 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Tri-Relief Antifungal
- Generic name (nonproprietary)
- sodium chloride, silicon dioxide, and thuja occidentalis leafy twig
- Active ingredients
- Sodium chloride — 10 [hp_X]/100mLSilicon dioxide — 10 [hp_X]/100mLThuja occidentalis leafy twig — 10 [hp_X]/100mL
- Dosage form
- Solution/ drops
- Route
- Topical
- Labeler
- Forces of NatureNDC labeler code 51393
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
- Identifiers
- Product ID 51393-7621_bbd2afbf-5951-471d-b3fd-923ea13bae8dSPL ID bbd2afbf-5951-471d-b3fd-923ea13bae8dSPL set ID 6fe97b54-8aa3-4d86-9055-0629589a416bUNII 451W47IQ8X, ETJ7Z6XBU4, 1NT28V9397
- Pharmacologic class
- Osmotic Laxative
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N451393762104followed by a unit qualifier and the quantityPackage 51393-7621-04. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses for relief from fungal infections, including ringworm, athlete's foot, and jock itch. Soothes itching, burning, and discomfort.
Excerpt only. Read the full label for complete information.
About NDC 51393-7621
- What is NDC 51393-7621?
- 51393-7621 is the product NDC for Tri-Relief Antifungal, Sodium chloride 10 [hp_X]/100mL + 2 more ingredients solution/ drops, listed with the FDA by Forces of Nature. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Tri-Relief Antifungal (SODIUM CHLORIDE, SILICON DIOXIDE, and THUJA OCCIDENTALIS LEAFY TWIG).
- What is the active ingredient?
- Sodium chloride, Silicon dioxide, Thuja occidentalis leafy twig.
- Who is the labeler?
- Forces of Nature, NDC labeler code 51393. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Tri-Relief Antifungal?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.