Melissa NDC 48951-7222

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-7222Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-7222Add 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
48951-7222-1	48951722201	10 g in 1 TUBE (48951-7222-1)Marketed from Sep 1, 2009

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): Melissa
Generic name (nonproprietary): melissa
Active ingredients: Melissa officinalis — 1 [hp_X]/gAconitum napellus — 30 [hp_X]/gToxicodendron pubescens leaf — 30 [hp_X]/gAtropa belladonna — 30 [hp_X]/g
Dosage form: Gel
Route: Topical
Labeler: Uriel Pharmacy, Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 1, 2009
Listing expires: Dec 31, 2026
Identifiers: Product ID 48951-7222_3eef31ef-39a4-3813-e063-6394a90a82afSPL ID 3eef31ef-39a4-3813-e063-6394a90a82afSPL set ID 3eef31ef-39a3-3813-e063-6394a90a82afUNII YF70189L0N, U0NQ8555JD, 6IO182RP7A, WQZ3G9PF0H

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

N448951722201 followed by a unit qualifier and the quantity

Package 48951-7222-01. 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 Sep 16, 2025.

Indications (excerpt from the label)

Directions: FOR TOPICAL USE ONLY.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)