NDC codes

FDA NDC Directory
Product NDC (as listed)51393-7621Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51393-7621Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
51393-7621-4513937621041 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

N451393762104 followed by a unit qualifier and the quantity

Package 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.

Full label on DailyMed (opens in a new tab)

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.

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