Arnica Nettle NDC 48951-1401

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-1401Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-1401Add 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
48951-1401-2	48951140102	60 g in 1 TUBE (48951-1401-2)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): Arnica Nettle
Generic name (nonproprietary): arnica nettle
Active ingredients: Calendula officinalis flowering top — 1 [hp_X]/gArnica montana flower — 1 [hp_X]/gThuja occidentalis whole — 1 [hp_X]/gUrtica urens — 1 [hp_X]/gComfrey root — 1 [hp_X]/gLytta vesicatoria — 5 [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 48951-1401_38cfb89f-3423-2c0b-e063-6394a90a33d8SPL ID 38cfb89f-3423-2c0b-e063-6394a90a33d8SPL set ID d694f7c5-050a-1883-e053-2995a90afc79UNII 18E7415PXQ, OZ0E5Y15PZ, 5HBV6WCE3N, IHN2NQ5OF9, M9VVZ08EKQ, 3Q034RO3BT

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

N448951140102 followed by a unit qualifier and the quantity

Package 48951-1401-02. 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 30, 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)