Artalgia NDC 45341-0002

NDC codes

FDA NDC Directory

Product NDC (as listed)45341-0002Labeler and product segments. Claims need a package NDC.

Product NDC at billing width45341-0002Add 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
45341-0002-1	45341000201	30 mL in 1 BOTTLE, DROPPER (45341-0002-1)Marketed from Jul 15, 2020

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): Artalgia
Generic name (nonproprietary): carduus marianus, arnica montana, agaricus muscarius, baryta carbonica, bellis perennis, glonoinum, hamamelis virginiana, mercurius solubilis, plumbum metallicum, secale cornutum, vanadium metallicum, carbo vegetabilis, hypericum perforatum, phosphorus pulsatilla (pratensis), rhus tox
Active ingredients: Milk thistle — 3 [hp_X]/mLArnica montana whole — 3 [hp_X]/mLAmanita muscaria fruiting body — 12 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLBellis perennis whole — 12 [hp_X]/mLNitroglycerin — 12 [hp_X]/mLHamamelis virginiana root bark/stem bark — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLLead — 12 [hp_X]/mLClaviceps purpurea sclerotium — 12 [hp_X]/mLVanadium — 12 [hp_X]/mLActivated charcoal — 30 [hp_X]/mLHypericum perforatum whole — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLPulsatilla pratensis whole — 30 [hp_X]/mLToxicodendron pubescens leaf — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Todd Horton DPM
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 15, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Nitrates (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 45341-0002_2c53f257-54a1-4a2b-aac3-6eaffea91603SPL ID 2c53f257-54a1-4a2b-aac3-6eaffea91603SPL set ID 9404b908-5b1c-44b0-a9ff-35f3768b8ed7UNII U946SH95EE, O80TY208ZW, DIF093I037, 6P669D8HQ8, 2HU33I03UY, G59M7S0WS3, T7S323PKJS, 324Y4038G2, 2P299V784P, 01G9XEA93N, 00J9J9XKDE, 2P3VWU3H10, XK4IUX8MNB, 27YLU75U4W, 8E272251DI, 6IO182RP7A
Pharmacologic class: Nitrate Vasodilator

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N445341000201 followed by a unit qualifier and the quantity

Package 45341-0002-01. 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 Jul 15, 2020.

Indications (excerpt from the label)

INDICATIONS AND USAGE: For temporary relief of numbness, tingling, discoloration, coldness, and burning of the lower extremities.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)