Advanced Arnica Plus NDC 57955-9979

NDC codes

FDA NDC Directory

Product NDC (as listed)57955-9979Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57955-9979Add 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
57955-9979-2	57955997902	59 mL in 1 BOTTLE, SPRAY (57955-9979-2)Marketed from Mar 15, 2026

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): Advanced Arnica Plus
Generic name (nonproprietary): arnica montana, arnica rad, bellis perennis, bryonia, hypericum perforatum, lithium carbonicum, magnesia phosphorica, phytolacca decandra, rhus tox, and ruta graveolens.
Active ingredients: Arnica montana whole — 10 [hp_X]/59mLArnica montana root — 10 [hp_X]/59mLBellis perennis whole — 10 [hp_X]/59mLBryonia alba root — 10 [hp_X]/59mLHypericum perforatum whole — 10 [hp_X]/59mLLithium carbonate — 10 [hp_X]/59mLMagnesium phosphate, Dibasic trihydrate — 10 [hp_X]/59mLPhytolacca americana root — 10 [hp_X]/59mLToxicodendron pubescens leaf — 10 [hp_X]/59mLRuta graveolens flowering top — 10 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: King Bio Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 15, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 57955-9979_c9f3c66e-e00f-4e62-beb4-5f73c663a9d0SPL ID c9f3c66e-e00f-4e62-beb4-5f73c663a9d0SPL set ID 8f1bac20-8403-4a15-bc29-f3bb1fa3c60dUNII O80TY208ZW, MUE8Y11327, 2HU33I03UY, T7J046YI2B, XK4IUX8MNB, 2BMD2GNA4V, HF539G9L3Q, 11E6VI8VEG, 6IO182RP7A, N94C2U587S
Pharmacologic class: Calculi Dissolution Agent; Mood Stabilizer; Osmotic Laxative

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

N457955997902 followed by a unit qualifier and the quantity

Package 57955-9979-02. 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

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