Nail Fungus Control Extra Strength NDC 51393-6989

NDC codes

FDA NDC Directory

Product NDC (as listed)51393-6989Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51393-6989Add 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 NDC	11-digit (billing)	Package
51393-6989-1	51393698901	11 mL in 1 BOTTLE, DISPENSING (51393-6989-1)Marketed from Apr 6, 2011
51393-6989-2	51393698902	33 mL in 1 BOTTLE, DISPENSING (51393-6989-2)Marketed from Apr 6, 2011
51393-6989-3	51393698903	30 mL in 1 BOTTLE, DISPENSING (51393-6989-3)Marketed from Jun 1, 2021

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): Nail Fungus Control Extra StrengthSuffix: Extra Strength
Generic name (nonproprietary): calendula officinalis flowering top, silicon dioxide, and hypericum perforatum
Active ingredients: Calendula officinalis flowering top — 8 [hp_X]/1000mLSilicon dioxide — 8 [hp_X]/1000mLHypericum perforatum whole — 8 [hp_X]/1000mL
Dosage form: Solution/ drops
Route: Topical
Labeler: Forces of Nature
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 6, 2011
Listing expires: Dec 31, 2027
Identifiers: Product ID 51393-6989_54417db2-c736-4d28-e063-6294a90a7643SPL ID 54417db2-c736-4d28-e063-6294a90a7643SPL set ID d02b88a6-1999-4dcd-91b5-fad88a664fcbUNII 18E7415PXQ, ETJ7Z6XBU4, XK4IUX8MNB

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

N451393698901 followed by a unit qualifier and the quantity

Package 51393-6989-01. 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 Jun 14, 2026.

Indications (excerpt from the label)

Uses for the relief and treatment of pain, soreness and inflammation from nail fungus. Symptoms: Discolored nails, Brittle nails, Distorted nails

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)