Alpha-Pro NDC 55346-0942

NDC codes

FDA NDC Directory

Product NDC (as listed)55346-0942Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55346-0942Add 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	Copy
55346-0942-1	55346094201	497 g in 1 BOTTLE (55346-0942-1)Marketed from Apr 1, 2013

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): Alpha-Pro
Generic name (nonproprietary): sodium fluoride and hydrofluoric acid
Active ingredients: Sodium fluoride — 7.9 mg/gHydrofluoric acid — 4.4 mg/g
Dosage form: Gel
Route: Dental
Labeler: Dental Technologies, Inc.
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Apr 1, 2013
Listing expires: Dec 31, 2026
Identifiers: Product ID 55346-0942_42c8ae03-7559-51a8-e063-6394a90ab69eSPL ID 42c8ae03-7559-51a8-e063-6394a90ab69eSPL set ID efe3646d-9eb1-4a49-aeb4-c4c224056851RxCUI 1297381UNII 8ZYQ1474W7, RGL5YE86CZ

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N455346094201 followed by a unit qualifier and the quantity

Package 55346-0942-01. 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 Nov 4, 2025.

Indications (excerpt from the label)

Indications and Usage: Topical application of APF gel is indicated in the prevention of dental caries. This treatment is normally used two times per year and should not exceed four times a year.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)